Canonical Allele Identifier: CA1769514598
Gene:

Linked Data

dbSNP Id: rs1799797209

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20735045A>T , CM000670.2:g.20735045A>T GRCh38
NC_000008.10:g.20592556A>T , CM000670.1:g.20592556A>T GRCh37
NC_000008.9:g.20636836A>T NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55401A>T