Canonical Allele Identifier: CA343774441
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs764695432
gnomAD v3: 1-173909834-G-C
gnomAD v4: 1-173909834-G-C
MyVariant Identifiers: chr1:g.173878972G>C (hg19) chr1:g.173909834G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909834G>C , CM000663.2:g.173909834G>C GRCh38
NC_000001.10:g.173878972G>C , CM000663.1:g.173878972G>C GRCh37
NC_000001.9:g.172145595G>C NCBI36
NG_012462.1:g.12545C>G , LRG_577:g.12545C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.871C>G MANE Select ENSP00000356671.3:p.Arg291Gly
ENST00000367698.3:c.871C>G ENSP00000356671.3:p.Arg291Gly
ENST00000487183.1:n.522C>G
ENST00000617423.4:c.559+2030C>G ENSP00000478688.1:n.559+2030C>G
NM_000488.3:c.871C>G , LRG_577t1:c.871C>G NP_000479.1:p.Arg291Gly
XM_005245198.2:c.727C>G XP_005245255.1:p.Arg243Gly
NM_001365052.1:c.727C>G NP_001351981.1:p.Arg243Gly
NM_000488.4:c.871C>G MANE Select NP_000479.1:p.Arg291Gly
NM_001365052.2:c.727C>G NP_001351981.1:p.Arg243Gly
NM_001386302.1:c.994C>G NP_001373231.1:p.Arg332Gly
NM_001386303.1:c.952C>G NP_001373232.1:p.Arg318Gly
NM_001386304.1:c.850C>G NP_001373233.1:p.Arg284Gly
NM_001386305.1:c.814C>G NP_001373234.1:p.Arg272Gly
NM_001386306.1:c.655C>G NP_001373235.1:p.Arg219Gly
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