Canonical Allele Identifier: CA362008132
Gene: SGCD HGNC NCBI

Linked Data

dbSNP Id: rs1437006739
gnomAD v4: 5-156508700-C-A
MyVariant Identifiers: chr5:g.155935710C>A (hg19) chr5:g.156508700C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.156508700C>A , CM000667.2:g.156508700C>A GRCh38
NC_000005.9:g.155935710C>A , CM000667.1:g.155935710C>A GRCh37
NC_000005.8:g.155868288C>A NCBI36
NG_008693.2:g.643357C>A , LRG_205:g.643357C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000337851.9:c.292C>A MANE Select ENSP00000338343.4:p.Pro98Thr
ENST00000337851.8:c.292C>A ENSP00000338343.4:p.Pro98Thr
ENST00000435422.7:c.289C>A ENSP00000403003.2:p.Pro97Thr
ENST00000517913.5:c.292C>A ENSP00000429378.1:p.Pro98Thr
ENST00000524347.2:c.*156C>A ENSP00000430794.1:n.*156C>A
NM_000337.5:c.292C>A , LRG_205t1:c.292C>A NP_000328.2:p.Pro98Thr
NM_001128209.1:c.289C>A NP_001121681.1:p.Pro97Thr
NM_172244.2:c.292C>A NP_758447.1:p.Pro98Thr
XM_005265966.3:c.292C>A XP_005266023.1:p.Pro98Thr
XM_005265967.1:c.292C>A XP_005266024.1:p.Pro98Thr
XM_006714911.2:c.292C>A XP_006714974.1:p.Pro98Thr
XM_011534621.1:c.289C>A XP_011532923.1:p.Pro97Thr
XM_005265966.5:c.292C>A XP_005266023.1:p.Pro98Thr
XM_005265967.2:c.292C>A XP_005266024.1:p.Pro98Thr
XM_011534621.2:c.289C>A XP_011532923.1:p.Pro97Thr
XM_017009723.2:c.292C>A XP_016865212.1:p.Pro98Thr
XM_017009724.1:c.292C>A XP_016865213.1:p.Pro98Thr
NM_001128209.2:c.289C>A NP_001121681.1:p.Pro97Thr
NM_172244.3:c.292C>A NP_758447.1:p.Pro98Thr
NM_000337.6:c.292C>A MANE Select NP_000328.2:p.Pro98Thr
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