Canonical Allele Identifier: CA527298257

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1336444125
• gnomAD v2: 1-173873007-G-C
• gnomAD v4: 1-173903869-G-C
• MyVariant Identifiers: chr1:g.173873007G>C (hg19) ; chr1:g.173903869G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173903869G>C , CM000663.2:g.173903869G>C	GRCh38
NC_000001.10:g.173873007G>C , CM000663.1:g.173873007G>C	GRCh37
NC_000001.9:g.172139630G>C	NCBI36
NG_012462.1:g.18510C>G , LRG_577:g.18510C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.*20C>G MANE Select	ENSP00000356671.3:n.*20C>G
ENST00000367698.3:c.*20C>G	ENSP00000356671.3:n.*20C>G
ENST00000617423.4:c.*20C>G	ENSP00000478688.1:n.*20C>G
NM_000488.3:c.*20C>G , LRG_577t1:c.*20C>G	NP_000479.1:n.*20C>G
XM_005245198.2:c.*20C>G	XP_005245255.1:n.*20C>G
NM_001365052.1:c.*20C>G	NP_001351981.1:n.*20C>G
NM_000488.4:c.*20C>G MANE Select	NP_000479.1:n.*20C>G
NM_001365052.2:c.*20C>G	NP_001351981.1:n.*20C>G
NM_001386302.1:c.*20C>G	NP_001373231.1:n.*20C>G
NM_001386303.1:c.*20C>G	NP_001373232.1:n.*20C>G
NM_001386304.1:c.*20C>G	NP_001373233.1:n.*20C>G
NM_001386305.1:c.*20C>G	NP_001373234.1:n.*20C>G
NM_001386306.1:c.*20C>G	NP_001373235.1:n.*20C>G