Canonical Allele Identifier: CA529370098
Gene:

Linked Data

dbSNP Id: rs544824096

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.224068660A>T , CM000663.2:g.224068660A>T GRCh38
NC_000001.10:g.224256362A>T , CM000663.1:g.224256362A>T GRCh37
NC_000001.9:g.222322985A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949173.1:n.385+1006A>T
XR_001737824.1:n.242+1006A>T