Canonical Allele Identifier: CA510163492
Gene: CST3 HGNC NCBI

Linked Data

MyVariant Identifiers: chr20:g.23618347A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23637710A>C , CM000682.2:g.23637710A>C GRCh38
NC_000020.10:g.23618347A>C , CM000682.1:g.23618347A>C GRCh37
NC_000020.9:g.23566347A>C NCBI36
NG_012887.2:g.5228T>G
NG_012887.3:g.5228T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000376925.8:c.153T>G MANE Select ENSP00000366124.3:p.Arg51=
ENST00000376925.7:c.153T>G ENSP00000366124.3:p.Arg51=
ENST00000398409.1:c.153T>G ENSP00000381446.1:p.Arg51=
ENST00000398411.5:c.153T>G ENSP00000381448.1:p.Arg51=
NM_000099.3:c.153T>G NP_000090.1:p.Arg51=
NM_001288614.1:c.153T>G NP_001275543.1:p.Arg51=
NM_000099.4:c.153T>G MANE Select NP_000090.1:p.Arg51=
NM_001288614.2:c.153T>G NP_001275543.1:p.Arg51=
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