Canonical Allele Identifier: CA1841175566
Gene:

Linked Data

dbSNP Id: rs1819676590

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551417G>A , CM000671.2:g.25551417G>A GRCh38
NC_000009.11:g.25551415G>A , CM000671.1:g.25551415G>A GRCh37
NC_000009.10:g.25541415G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-845C>T
XR_929525.2:n.674-845C>T