Canonical Allele Identifier: CA1009277711

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1657715762
• gnomAD v3: 1-173910352-G-A
• gnomAD v4: 1-173910352-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173910352G>A , CM000663.2:g.173910352G>A	GRCh38
NC_000001.10:g.173879490G>A , CM000663.1:g.173879490G>A	GRCh37
NC_000001.9:g.172146113G>A	NCBI36
NG_012462.1:g.12027C>T , LRG_577:g.12027C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.762+402C>T MANE Select	ENSP00000356671.3:n.762+402C>T
ENST00000367698.3:c.762+402C>T	ENSP00000356671.3:n.762+402C>T
ENST00000487183.1:n.413+402C>T
ENST00000617423.4:c.559+1512C>T	ENSP00000478688.1:n.559+1512C>T
NM_000488.3:c.762+402C>T , LRG_577t1:c.762+402C>T	NP_000479.1:n.762+402C>T
XM_005245198.2:c.618+402C>T	XP_005245255.1:n.618+402C>T
NM_001365052.1:c.618+402C>T	NP_001351981.1:n.618+402C>T
NM_000488.4:c.762+402C>T MANE Select	NP_000479.1:n.762+402C>T
NM_001365052.2:c.618+402C>T	NP_001351981.1:n.618+402C>T
NM_001386302.1:c.885+279C>T	NP_001373231.1:n.885+279C>T
NM_001386303.1:c.843+402C>T	NP_001373232.1:n.843+402C>T
NM_001386304.1:c.742-410C>T	NP_001373233.1:n.742-410C>T
NM_001386305.1:c.762+402C>T	NP_001373234.1:n.762+402C>T
NM_001386306.1:c.546+402C>T	NP_001373235.1:n.546+402C>T