Canonical Allele Identifier: CA9790249
Gene: CST3 HGNC NCBI

Linked Data

dbSNP Id: rs750555631

Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23637667C>T , CM000682.2:g.23637667C>T GRCh38
NC_000020.10:g.23618304C>T , CM000682.1:g.23618304C>T GRCh37
NC_000020.9:g.23566304C>T NCBI36
NG_012887.2:g.5271G>A
NG_012887.3:g.5271G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376925.8:c.196G>A MANE Select ENSP00000366124.3:p.Asp66Asn
ENST00000376925.7:c.196G>A ENSP00000366124.3:p.Asp66Asn
ENST00000398409.1:c.196G>A ENSP00000381446.1:p.Asp66Asn
ENST00000398411.5:c.196G>A ENSP00000381448.1:p.Asp66Asn
NM_000099.3:c.196G>A NP_000090.1:p.Asp66Asn
NM_001288614.1:c.196G>A NP_001275543.1:p.Asp66Asn
NM_000099.4:c.196G>A MANE Select NP_000090.1:p.Asp66Asn
NM_001288614.2:c.196G>A NP_001275543.1:p.Asp66Asn