Canonical Allele Identifier: CA891313843

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1391295579
• gnomAD v3: 1-173910354-A-G
• gnomAD v4: 1-173910354-A-G
• MyVariant Identifiers: chr1:g.173879492A>G (hg19) ; chr1:g.173910354A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173910354A>G , CM000663.2:g.173910354A>G	GRCh38
NC_000001.10:g.173879492A>G , CM000663.1:g.173879492A>G	GRCh37
NC_000001.9:g.172146115A>G	NCBI36
NG_012462.1:g.12025T>C , LRG_577:g.12025T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.762+400T>C MANE Select	ENSP00000356671.3:n.762+400T>C
ENST00000367698.3:c.762+400T>C	ENSP00000356671.3:n.762+400T>C
ENST00000487183.1:n.413+400T>C
ENST00000617423.4:c.559+1510T>C	ENSP00000478688.1:n.559+1510T>C
NM_000488.3:c.762+400T>C , LRG_577t1:c.762+400T>C	NP_000479.1:n.762+400T>C
XM_005245198.2:c.618+400T>C	XP_005245255.1:n.618+400T>C
NM_001365052.1:c.618+400T>C	NP_001351981.1:n.618+400T>C
NM_000488.4:c.762+400T>C MANE Select	NP_000479.1:n.762+400T>C
NM_001365052.2:c.618+400T>C	NP_001351981.1:n.618+400T>C
NM_001386302.1:c.885+277T>C	NP_001373231.1:n.885+277T>C
NM_001386303.1:c.843+400T>C	NP_001373232.1:n.843+400T>C
NM_001386304.1:c.742-412T>C	NP_001373233.1:n.742-412T>C
NM_001386305.1:c.762+400T>C	NP_001373234.1:n.762+400T>C
NM_001386306.1:c.546+400T>C	NP_001373235.1:n.546+400T>C