Canonical Allele Identifier: CA1841175492
Gene:

Linked Data

dbSNP Id: rs1462723151

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.25551276G>C , CM000671.2:g.25551276G>C GRCh38
NC_000009.11:g.25551274G>C , CM000671.1:g.25551274G>C GRCh37
NC_000009.10:g.25541274G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_929525.1:n.50-704C>G
XR_929525.2:n.674-704C>G