Canonical Allele Identifier: CA32777215

Gene: SERPINC1

Linked Data

• dbSNP Id: rs904717916
• MyVariant Identifiers: chr1:g.173873023C>A (hg19) ; chr1:g.173903885C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903885C>A , CM000663.2:g.173903885C>A	GRCh38
NC_000001.10:g.173873023C>A , CM000663.1:g.173873023C>A	GRCh37
NC_000001.9:g.172139646C>A	NCBI36
NG_012462.1:g.18494G>T , LRG_577:g.18494G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.*4G>T MANE Select	ENSP00000356671.3:n.*4G>T
ENST00000367698.3:c.*4G>T	ENSP00000356671.3:n.*4G>T
ENST00000617423.4:c.*4G>T	ENSP00000478688.1:n.*4G>T
NM_000488.3:c.*4G>T , LRG_577t1:c.*4G>T	NP_000479.1:n.*4G>T
XM_005245198.2:c.*4G>T	XP_005245255.1:n.*4G>T
NM_001365052.1:c.*4G>T	NP_001351981.1:n.*4G>T
NM_000488.4:c.*4G>T MANE Select	NP_000479.1:n.*4G>T
NM_001365052.2:c.*4G>T	NP_001351981.1:n.*4G>T
NM_001386302.1:c.*4G>T	NP_001373231.1:n.*4G>T
NM_001386303.1:c.*4G>T	NP_001373232.1:n.*4G>T
NM_001386304.1:c.*4G>T	NP_001373233.1:n.*4G>T
NM_001386305.1:c.*4G>T	NP_001373234.1:n.*4G>T
NM_001386306.1:c.*4G>T	NP_001373235.1:n.*4G>T