Canonical Allele Identifier: CA32781078

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1039556890
• gnomAD v3: 1-173911300-G-A
• gnomAD v4: 1-173911300-G-A
• MyVariant Identifiers: chr1:g.173880438G>A (hg19) ; chr1:g.173911300G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911300G>A , CM000663.2:g.173911300G>A	GRCh38
NC_000001.10:g.173880438G>A , CM000663.1:g.173880438G>A	GRCh37
NC_000001.9:g.172147061G>A	NCBI36
NG_012462.1:g.11079C>T , LRG_577:g.11079C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367698.4:c.625-409C>T MANE Select	ENSP00000356671.3:n.625-409C>T
ENST00000367698.3:c.625-409C>T	ENSP00000356671.3:n.625-409C>T
ENST00000487183.1:n.330-463C>T
ENST00000617423.4:c.559+564C>T	ENSP00000478688.1:n.559+564C>T
NM_000488.3:c.625-409C>T , LRG_577t1:c.625-409C>T	NP_000479.1:n.625-409C>T
XM_005245198.2:c.481-409C>T	XP_005245255.1:n.481-409C>T
NM_001365052.1:c.481-409C>T	NP_001351981.1:n.481-409C>T
NM_000488.4:c.625-409C>T MANE Select	NP_000479.1:n.625-409C>T
NM_001365052.2:c.481-409C>T	NP_001351981.1:n.481-409C>T
NM_001386302.1:c.625-409C>T	NP_001373231.1:n.625-409C>T
NM_001386303.1:c.706-409C>T	NP_001373232.1:n.706-409C>T
NM_001386304.1:c.625-409C>T	NP_001373233.1:n.625-409C>T
NM_001386305.1:c.625-409C>T	NP_001373234.1:n.625-409C>T
NM_001386306.1:c.409-409C>T	NP_001373235.1:n.409-409C>T