Canonical Allele Identifier: CA146023669
Gene:

Identifiers and link-outs to other resources

dbSNP Id: rs17635492

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.117450114A>T , CM000668.2:g.117450114A>T GRCh38
NC_000006.11:g.117771277A>T , CM000668.1:g.117771277A>T GRCh37
NC_000006.10:g.117877970A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000467125.1:n.547+116740T>A ENSP00000487717.1:p.=