Canonical Allele Identifier: CA422484289
Gene:

Linked Data

dbSNP Id: rs1328183922

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.192800580G>A , CM000663.2:g.192800580G>A GRCh38
NC_000001.10:g.192769710G>A , CM000663.1:g.192769710G>A GRCh37
NC_000001.9:g.191036333G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000429211.2:n.10G>A