Canonical Allele Identifier: CA15133095

Gene: SERPINC1

Linked Data

• ClinVar Variation Id: 1287399
• ClinVar RCV Id: RCV001710526
• dbSNP Id: rs2227589
• gnomAD v2: 1-173886216-C-T
• gnomAD v3: 1-173917078-C-T
• gnomAD v4: 1-173917078-C-T
• MyVariant Identifiers: chr1:g.173886216C>T (hg19) ; chr1:g.173917078C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173917078C>T , CM000663.2:g.173917078C>T	GRCh38
NC_000001.10:g.173886216C>T , CM000663.1:g.173886216C>T	GRCh37
NC_000001.9:g.172152839C>T	NCBI36
NG_012462.1:g.5301G>A , LRG_577:g.5301G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.41+141G>A MANE Select	ENSP00000356671.3:n.41+141G>A
ENST00000367698.3:c.41+141G>A	ENSP00000356671.3:n.41+141G>A
ENST00000494024.1:n.98+141G>A
ENST00000617423.4:c.41+141G>A	ENSP00000478688.1:n.41+141G>A
NM_000488.3:c.41+141G>A , LRG_577t1:c.41+141G>A	NP_000479.1:n.41+141G>A
XM_005245198.2:c.-273+141G>A	XP_005245255.1:n.-273+141G>A
NM_001365052.1:c.-273+141G>A	NP_001351981.1:n.-273+141G>A
NM_000488.4:c.41+141G>A MANE Select	NP_000479.1:n.41+141G>A
NM_001365052.2:c.-273+141G>A	NP_001351981.1:n.-273+141G>A
NM_001386302.1:c.41+141G>A	NP_001373231.1:n.41+141G>A
NM_001386303.1:c.24+158G>A	NP_001373232.1:n.24+158G>A
NM_001386304.1:c.41+141G>A	NP_001373233.1:n.41+141G>A
NM_001386305.1:c.41+141G>A	NP_001373234.1:n.41+141G>A
NM_001386306.1:c.41+141G>A	NP_001373235.1:n.41+141G>A