Canonical Allele Identifier: CA891313815

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1356910431
• gnomAD v3: 1-173910345-G-A
• gnomAD v4: 1-173910345-G-A
• MyVariant Identifiers: chr1:g.173879483G>A (hg19) ; chr1:g.173910345G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173910345G>A , CM000663.2:g.173910345G>A	GRCh38
NC_000001.10:g.173879483G>A , CM000663.1:g.173879483G>A	GRCh37
NC_000001.9:g.172146106G>A	NCBI36
NG_012462.1:g.12034C>T , LRG_577:g.12034C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.763-403C>T MANE Select	ENSP00000356671.3:n.763-403C>T
ENST00000367698.3:c.763-403C>T	ENSP00000356671.3:n.763-403C>T
ENST00000487183.1:n.414-403C>T
ENST00000617423.4:c.559+1519C>T	ENSP00000478688.1:n.559+1519C>T
NM_000488.3:c.763-403C>T , LRG_577t1:c.763-403C>T	NP_000479.1:n.763-403C>T
XM_005245198.2:c.619-403C>T	XP_005245255.1:n.619-403C>T
NM_001365052.1:c.619-403C>T	NP_001351981.1:n.619-403C>T
NM_000488.4:c.763-403C>T MANE Select	NP_000479.1:n.763-403C>T
NM_001365052.2:c.619-403C>T	NP_001351981.1:n.619-403C>T
NM_001386302.1:c.885+286C>T	NP_001373231.1:n.885+286C>T
NM_001386303.1:c.844-403C>T	NP_001373232.1:n.844-403C>T
NM_001386304.1:c.742-403C>T	NP_001373233.1:n.742-403C>T
NM_001386305.1:c.762+409C>T	NP_001373234.1:n.762+409C>T
NM_001386306.1:c.547-403C>T	NP_001373235.1:n.547-403C>T