Canonical Allele Identifier: CA343774243
Gene: SERPINC1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.173878921C>A (hg19) chr1:g.173909783C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909783C>A , CM000663.2:g.173909783C>A GRCh38
NC_000001.10:g.173878921C>A , CM000663.1:g.173878921C>A GRCh37
NC_000001.9:g.172145544C>A NCBI36
NG_012462.1:g.12596G>T , LRG_577:g.12596G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.922G>T MANE Select ENSP00000356671.3:p.Gly308Cys
ENST00000367698.3:c.922G>T ENSP00000356671.3:p.Gly308Cys
ENST00000487183.1:n.573G>T
ENST00000617423.4:c.559+2081G>T ENSP00000478688.1:n.559+2081G>T
NM_000488.3:c.922G>T , LRG_577t1:c.922G>T NP_000479.1:p.Gly308Cys
XM_005245198.2:c.778G>T XP_005245255.1:p.Gly260Cys
NM_001365052.1:c.778G>T NP_001351981.1:p.Gly260Cys
NM_000488.4:c.922G>T MANE Select NP_000479.1:p.Gly308Cys
NM_001365052.2:c.778G>T NP_001351981.1:p.Gly260Cys
NM_001386302.1:c.1045G>T NP_001373231.1:p.Gly349Cys
NM_001386303.1:c.1003G>T NP_001373232.1:p.Gly335Cys
NM_001386304.1:c.901G>T NP_001373233.1:p.Gly301Cys
NM_001386305.1:c.865G>T NP_001373234.1:p.Gly289Cys
NM_001386306.1:c.706G>T NP_001373235.1:p.Gly236Cys
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