Canonical Allele Identifier: CA1207936318

Gene: SERPINC1

Linked Data

• dbSNP Id: rs1413626505

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.173908277G>C , CM000663.2:g.173908277G>C	GRCh38
NC_000001.10:g.173877415G>C , CM000663.1:g.173877415G>C	GRCh37
NC_000001.9:g.172144038G>C	NCBI36
NG_012462.1:g.14102C>G , LRG_577:g.14102C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000367698.4:c.1154-763C>G MANE Select	ENSP00000356671.3:n.1154-763C>G
ENST00000367698.3:c.1154-763C>G	ENSP00000356671.3:n.1154-763C>G
ENST00000617423.4:c.560-784C>G	ENSP00000478688.1:n.560-784C>G
NM_000488.3:c.1154-763C>G , LRG_577t1:c.1154-763C>G	NP_000479.1:n.1154-763C>G
XM_005245198.2:c.1010-763C>G	XP_005245255.1:n.1010-763C>G
NM_001365052.1:c.1010-763C>G	NP_001351981.1:n.1010-763C>G
NM_000488.4:c.1154-763C>G MANE Select	NP_000479.1:n.1154-763C>G
NM_001365052.2:c.1010-763C>G	NP_001351981.1:n.1010-763C>G
NM_001386302.1:c.1277-763C>G	NP_001373231.1:n.1277-763C>G
NM_001386303.1:c.1235-763C>G	NP_001373232.1:n.1235-763C>G
NM_001386304.1:c.1133-763C>G	NP_001373233.1:n.1133-763C>G
NM_001386305.1:c.1097-763C>G	NP_001373234.1:n.1097-763C>G
NM_001386306.1:c.938-763C>G	NP_001373235.1:n.938-763C>G