Canonical Allele Identifier: CA614218579
Gene:

Linked Data

dbSNP Id: rs1407676485

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.52417643T>G , CM000676.2:g.52417643T>G GRCh38
NC_000014.8:g.52884361T>G , CM000676.1:g.52884361T>G GRCh37
NC_000014.7:g.51954111T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943866.1:n.3060A>C