Canonical Allele Identifier: CA1769514524
Gene:

Linked Data

dbSNP Id: rs1799795975

Genomic Alleles

HGVS Genome Assembly
NC_000008.11:g.20734907T>G , CM000670.2:g.20734907T>G GRCh38
NC_000008.10:g.20592418T>G , CM000670.1:g.20592418T>G GRCh37
NC_000008.9:g.20636698T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_949569.3:n.72-55539T>G