Canonical Allele Identifier: CA421823043

Gene: SERPINC1

Linked Data

• dbSNP Id: rs2102786004
• gnomAD v3: 1-173911901-T-C
• gnomAD v4: 1-173911901-T-C
• MyVariant Identifiers: chr1:g.173881039T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173911901T>C , CM000663.2:g.173911901T>C	GRCh38
NC_000001.10:g.173881039T>C , CM000663.1:g.173881039T>C	GRCh37
NC_000001.9:g.172147662T>C	NCBI36
NG_012462.1:g.10478A>G , LRG_577:g.10478A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.522A>G MANE Select	ENSP00000356671.3:p.Ser174=
ENST00000367698.3:c.522A>G	ENSP00000356671.3:p.Ser174=
ENST00000487183.1:n.227A>G
ENST00000617423.4:c.522A>G	ENSP00000478688.1:p.Ser174=
NM_000488.3:c.522A>G , LRG_577t1:c.522A>G	NP_000479.1:p.Ser174=
XM_005245198.2:c.378A>G	XP_005245255.1:p.Ser126=
NM_001365052.1:c.378A>G	NP_001351981.1:p.Ser126=
NM_000488.4:c.522A>G MANE Select	NP_000479.1:p.Ser174=
NM_001365052.2:c.378A>G	NP_001351981.1:p.Ser126=
NM_001386302.1:c.522A>G	NP_001373231.1:p.Ser174=
NM_001386303.1:c.603A>G	NP_001373232.1:p.Ser201=
NM_001386304.1:c.522A>G	NP_001373233.1:p.Ser174=
NM_001386305.1:c.522A>G	NP_001373234.1:p.Ser174=
NM_001386306.1:c.409-1010A>G	NP_001373235.1:n.409-1010A>G