Canonical Allele Identifier: CA421942817

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1479495380
• gnomAD v3: 1-173909592-G-T
• gnomAD v4: 1-173909592-G-T
• MyVariant Identifiers: chr1:g.173878730G>T (hg19) ; chr1:g.173909592G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909592G>T , CM000663.2:g.173909592G>T	GRCh38
NC_000001.10:g.173878730G>T , CM000663.1:g.173878730G>T	GRCh37
NC_000001.9:g.172145353G>T	NCBI36
NG_012462.1:g.12787C>A , LRG_577:g.12787C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.1113C>A MANE Select	ENSP00000356671.3:p.Gly371=
ENST00000367698.3:c.1113C>A	ENSP00000356671.3:p.Gly371=
ENST00000617423.4:c.560-2099C>A	ENSP00000478688.1:n.560-2099C>A
NM_000488.3:c.1113C>A , LRG_577t1:c.1113C>A	NP_000479.1:p.Gly371=
XM_005245198.2:c.969C>A	XP_005245255.1:p.Gly323=
NM_001365052.1:c.969C>A	NP_001351981.1:p.Gly323=
NM_000488.4:c.1113C>A MANE Select	NP_000479.1:p.Gly371=
NM_001365052.2:c.969C>A	NP_001351981.1:p.Gly323=
NM_001386302.1:c.1236C>A	NP_001373231.1:p.Gly412=
NM_001386303.1:c.1194C>A	NP_001373232.1:p.Gly398=
NM_001386304.1:c.1092C>A	NP_001373233.1:p.Gly364=
NM_001386305.1:c.1056C>A	NP_001373234.1:p.Gly352=
NM_001386306.1:c.897C>A	NP_001373235.1:p.Gly299=