Canonical Allele Identifier: CA362008136
Gene: SGCD HGNC NCBI

Linked Data

dbSNP Id: rs2127875640
gnomAD v3: 5-156508701-C-G
gnomAD v4: 5-156508701-C-G
MyVariant Identifiers: chr5:g.155935711C>G (hg19) chr5:g.156508701C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156508701C>G , CM000667.2:g.156508701C>G GRCh38
NC_000005.9:g.155935711C>G , CM000667.1:g.155935711C>G GRCh37
NC_000005.8:g.155868289C>G NCBI36
NG_008693.2:g.643358C>G , LRG_205:g.643358C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000337851.9:c.293C>G MANE Select ENSP00000338343.4:p.Pro98Arg
ENST00000337851.8:c.293C>G ENSP00000338343.4:p.Pro98Arg
ENST00000435422.7:c.290C>G ENSP00000403003.2:p.Pro97Arg
ENST00000517913.5:c.293C>G ENSP00000429378.1:p.Pro98Arg
ENST00000524347.2:c.*157C>G ENSP00000430794.1:n.*157C>G
NM_000337.5:c.293C>G , LRG_205t1:c.293C>G NP_000328.2:p.Pro98Arg
NM_001128209.1:c.290C>G NP_001121681.1:p.Pro97Arg
NM_172244.2:c.293C>G NP_758447.1:p.Pro98Arg
XM_005265966.3:c.293C>G XP_005266023.1:p.Pro98Arg
XM_005265967.1:c.293C>G XP_005266024.1:p.Pro98Arg
XM_006714911.2:c.293C>G XP_006714974.1:p.Pro98Arg
XM_011534621.1:c.290C>G XP_011532923.1:p.Pro97Arg
XM_005265966.5:c.293C>G XP_005266023.1:p.Pro98Arg
XM_005265967.2:c.293C>G XP_005266024.1:p.Pro98Arg
XM_011534621.2:c.290C>G XP_011532923.1:p.Pro97Arg
XM_017009723.2:c.293C>G XP_016865212.1:p.Pro98Arg
XM_017009724.1:c.293C>G XP_016865213.1:p.Pro98Arg
NM_001128209.2:c.290C>G NP_001121681.1:p.Pro97Arg
NM_172244.3:c.293C>G NP_758447.1:p.Pro98Arg
NM_000337.6:c.293C>G MANE Select NP_000328.2:p.Pro98Arg
Search 100 bp 5'
Search 100 bp 3'