Canonical Allele Identifier: CA2355967032
Gene: CST3 HGNC NCBI

Linked Data

dbSNP Id: rs368971982
gnomAD v4: 20-23637609-G-T
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Genomic Alleles

HGVS Genome Assembly
NC_000020.11:g.23637609G>T , CM000682.2:g.23637609G>T GRCh38
NC_000020.10:g.23618246G>T , CM000682.1:g.23618246G>T GRCh37
NC_000020.9:g.23566246G>T NCBI36
NG_012887.2:g.5329C>A
NG_012887.3:g.5329C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000376925.8:c.243+11C>A MANE Select ENSP00000366124.3:n.243+11C>A
ENST00000376925.7:c.243+11C>A ENSP00000366124.3:n.243+11C>A
ENST00000398409.1:c.243+11C>A ENSP00000381446.1:n.243+11C>A
ENST00000398411.5:c.243+11C>A ENSP00000381448.1:n.243+11C>A
NM_000099.3:c.243+11C>A NP_000090.1:n.243+11C>A
NM_001288614.1:c.243+11C>A NP_001275543.1:n.243+11C>A
NM_000099.4:c.243+11C>A MANE Select NP_000090.1:n.243+11C>A
NM_001288614.2:c.243+11C>A NP_001275543.1:n.243+11C>A
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