Canonical Allele Identifier: CA210795
Gene: SERPINC1 HGNC NCBI

Linked Data

ClinVar Variation Id: 18041
ClinVar RCV Id: RCV000019657
dbSNP Id: rs121909570

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.173911923T>G , CM000663.2:g.173911923T>G GRCh38
NC_000001.10:g.173881061T>G , CM000663.1:g.173881061T>G GRCh37
NC_000001.9:g.172147684T>G NCBI36
NG_012462.1:g.10456A>C , LRG_577:g.10456A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000367698.4:c.500A>C MANE Select ENSP00000356671.3:p.Asn167Thr
ENST00000367698.3:c.500A>C ENSP00000356671.3:p.Asn167Thr
ENST00000487183.1:n.205A>C
ENST00000617423.4:c.500A>C ENSP00000478688.1:p.Asn167Thr
NM_000488.3:c.500A>C , LRG_577t1:c.500A>C NP_000479.1:p.Asn167Thr
XM_005245198.2:c.356A>C XP_005245255.1:p.Asn119Thr
NM_001365052.1:c.356A>C NP_001351981.1:p.Asn119Thr
NM_000488.4:c.500A>C MANE Select NP_000479.1:p.Asn167Thr
NM_001365052.2:c.356A>C NP_001351981.1:p.Asn119Thr
NM_001386302.1:c.500A>C NP_001373231.1:p.Asn167Thr
NM_001386303.1:c.581A>C NP_001373232.1:p.Asn194Thr
NM_001386304.1:c.500A>C NP_001373233.1:p.Asn167Thr
NM_001386305.1:c.500A>C NP_001373234.1:p.Asn167Thr
NM_001386306.1:c.409-1032A>C NP_001373235.1:p.=