Canonical Allele Identifier: CA1769514544
Gene:

Linked Data

dbSNP Id: rs1799796250

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20734945A>T , CM000670.2:g.20734945A>T GRCh38
NC_000008.10:g.20592456A>T , CM000670.1:g.20592456A>T GRCh37
NC_000008.9:g.20636736A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55501A>T