Canonical Allele Identifier: CA1251222

Gene: SERPINC1

Linked Data

• dbSNP Id: rs767159321
• ExAC: 1:173873150 G / T
• gnomAD v2: 1-173873150-G-T
• MyVariant Identifiers: chr1:g.173873150G>T (hg19) ; chr1:g.173904012G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173904012G>T , CM000663.2:g.173904012G>T	GRCh38
NC_000001.10:g.173873150G>T , CM000663.1:g.173873150G>T	GRCh37
NC_000001.9:g.172139773G>T	NCBI36
NG_012462.1:g.18367C>A , LRG_577:g.18367C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1272C>A MANE Select	ENSP00000356671.3:p.Gly424=
ENST00000367698.3:c.1272C>A	ENSP00000356671.3:p.Gly424=
ENST00000617423.4:c.657C>A	ENSP00000478688.1:p.Gly219=
NM_000488.3:c.1272C>A , LRG_577t1:c.1272C>A	NP_000479.1:p.Gly424=
XM_005245198.2:c.1128C>A	XP_005245255.1:p.Gly376=
NM_001365052.1:c.1128C>A	NP_001351981.1:p.Gly376=
NM_000488.4:c.1272C>A MANE Select	NP_000479.1:p.Gly424=
NM_001365052.2:c.1128C>A	NP_001351981.1:p.Gly376=
NM_001386302.1:c.1395C>A	NP_001373231.1:p.Gly465=
NM_001386303.1:c.1353C>A	NP_001373232.1:p.Gly451=
NM_001386304.1:c.1251C>A	NP_001373233.1:p.Gly417=
NM_001386305.1:c.1215C>A	NP_001373234.1:p.Gly405=
NM_001386306.1:c.1056C>A	NP_001373235.1:p.Gly352=