Canonical Allele Identifier: CA2605585999
Gene:

Linked Data

dbSNP Id: rs145817397

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.168649495C>A , CM000663.2:g.168649495C>A GRCh38
NC_000001.10:g.168618733C>A , CM000663.1:g.168618733C>A GRCh37
NC_000001.9:g.166885357C>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_922259.1:n.201-8220G>T
XR_922259.2:n.332-8220G>T