Canonical Allele Identifier: CA421942745

Gene: SERPINC1

Linked Data

• dbSNP Id: rs776662899
• gnomAD v2: 1-173878966-G-T
• gnomAD v4: 1-173909828-G-T
• MyVariant Identifiers: chr1:g.173878966G>T (hg19) ; chr1:g.173909828G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173909828G>T , CM000663.2:g.173909828G>T	GRCh38
NC_000001.10:g.173878966G>T , CM000663.1:g.173878966G>T	GRCh37
NC_000001.9:g.172145589G>T	NCBI36
NG_012462.1:g.12551C>A , LRG_577:g.12551C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.877C>A MANE Select	ENSP00000356671.3:p.Arg293=
ENST00000367698.3:c.877C>A	ENSP00000356671.3:p.Arg293=
ENST00000487183.1:n.528C>A
ENST00000617423.4:c.559+2036C>A	ENSP00000478688.1:n.559+2036C>A
NM_000488.3:c.877C>A , LRG_577t1:c.877C>A	NP_000479.1:p.Arg293=
XM_005245198.2:c.733C>A	XP_005245255.1:p.Arg245=
NM_001365052.1:c.733C>A	NP_001351981.1:p.Arg245=
NM_000488.4:c.877C>A MANE Select	NP_000479.1:p.Arg293=
NM_001365052.2:c.733C>A	NP_001351981.1:p.Arg245=
NM_001386302.1:c.1000C>A	NP_001373231.1:p.Arg334=
NM_001386303.1:c.958C>A	NP_001373232.1:p.Arg320=
NM_001386304.1:c.856C>A	NP_001373233.1:p.Arg286=
NM_001386305.1:c.820C>A	NP_001373234.1:p.Arg274=
NM_001386306.1:c.661C>A	NP_001373235.1:p.Arg221=