Canonical Allele Identifier: CA1251287
Gene: SERPINC1 HGNC NCBI

Linked Data

dbSNP Id: rs373515340

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173909638C>T , CM000663.2:g.173909638C>T GRCh38
NC_000001.10:g.173878776C>T , CM000663.1:g.173878776C>T GRCh37
NC_000001.9:g.172145399C>T NCBI36
NG_012462.1:g.12741G>A , LRG_577:g.12741G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000367698.4:c.1067G>A MANE Select ENSP00000356671.3:p.Arg356His
ENST00000367698.3:c.1067G>A ENSP00000356671.3:p.Arg356His
ENST00000617423.4:c.560-2145G>A ENSP00000478688.1:n.560-2145G>A
NM_000488.3:c.1067G>A , LRG_577t1:c.1067G>A NP_000479.1:p.Arg356His
XM_005245198.2:c.923G>A XP_005245255.1:p.Arg308His
NM_001365052.1:c.923G>A NP_001351981.1:p.Arg308His
NM_000488.4:c.1067G>A MANE Select NP_000479.1:p.Arg356His
NM_001365052.2:c.923G>A NP_001351981.1:p.Arg308His
NM_001386302.1:c.1190G>A NP_001373231.1:p.Arg397His
NM_001386303.1:c.1148G>A NP_001373232.1:p.Arg383His
NM_001386304.1:c.1046G>A NP_001373233.1:p.Arg349His
NM_001386305.1:c.1010G>A NP_001373234.1:p.Arg337His
NM_001386306.1:c.851G>A NP_001373235.1:p.Arg284His