Canonical Allele Identifier: CA32783285

Gene: SERPINC1

Linked Data

• dbSNP Id: rs896860865
• gnomAD v4: 1-173917164-T-C
• MyVariant Identifiers: chr1:g.173886302T>C (hg19) ; chr1:g.173917164T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173917164T>C , CM000663.2:g.173917164T>C	GRCh38
NC_000001.10:g.173886302T>C , CM000663.1:g.173886302T>C	GRCh37
NC_000001.9:g.172152925T>C	NCBI36
NG_012462.1:g.5215A>G , LRG_577:g.5215A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.41+55A>G MANE Select	ENSP00000356671.3:n.41+55A>G
ENST00000367698.3:c.41+55A>G	ENSP00000356671.3:n.41+55A>G
ENST00000494024.1:n.98+55A>G
ENST00000617423.4:c.41+55A>G	ENSP00000478688.1:n.41+55A>G
NM_000488.3:c.41+55A>G , LRG_577t1:c.41+55A>G	NP_000479.1:n.41+55A>G
XM_005245198.2:c.-273+55A>G	XP_005245255.1:n.-273+55A>G
NM_001365052.1:c.-273+55A>G	NP_001351981.1:n.-273+55A>G
NM_000488.4:c.41+55A>G MANE Select	NP_000479.1:n.41+55A>G
NM_001365052.2:c.-273+55A>G	NP_001351981.1:n.-273+55A>G
NM_001386302.1:c.41+55A>G	NP_001373231.1:n.41+55A>G
NM_001386303.1:c.24+72A>G	NP_001373232.1:n.24+72A>G
NM_001386304.1:c.41+55A>G	NP_001373233.1:n.41+55A>G
NM_001386305.1:c.41+55A>G	NP_001373234.1:n.41+55A>G
NM_001386306.1:c.41+55A>G	NP_001373235.1:n.41+55A>G