Canonical Allele Identifier: CA210785
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 18033
ClinVar RCV Id: RCV000019649
dbSNP Id: rs121909566

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173904013C>T , CM000663.2:g.173904013C>T GRCh38
NC_000001.10:g.173873151C>T , CM000663.1:g.173873151C>T GRCh37
NC_000001.9:g.172139774C>T NCBI36
NG_012462.1:g.18366G>A , LRG_577:g.18366G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.3:c.1271G>A ENSP00000356671.3:p.Gly424Asp
ENST00000617423.4:c.656G>A ENSP00000478688.1:p.Gly219Asp
NM_000488.3:c.1271G>A , LRG_577t1:c.1271G>A NP_000479.1:p.Gly424Asp
XM_005245198.2:c.1127G>A XP_005245255.1:p.Gly376Asp
NM_001365052.1:c.1127G>A NP_001351981.1:p.Gly376Asp
NM_000488.4:c.1271G>A MANE Select NP_000479.1:p.Gly424Asp
NM_001365052.2:c.1127G>A NP_001351981.1:p.Gly376Asp
NM_001386302.1:c.1394G>A NP_001373231.1:p.Gly465Asp
NM_001386303.1:c.1352G>A NP_001373232.1:p.Gly451Asp
NM_001386304.1:c.1250G>A NP_001373233.1:p.Gly417Asp
NM_001386305.1:c.1214G>A NP_001373234.1:p.Gly405Asp
NM_001386306.1:c.1055G>A NP_001373235.1:p.Gly352Asp