Canonical Allele Identifier: CA59107087
Gene:

Linked Data

dbSNP Id: rs970563021

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870610T>G , CM000664.2:g.155870610T>G GRCh38
NC_000002.11:g.156727122T>G , CM000664.1:g.156727122T>G GRCh37
NC_000002.10:g.156435368T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_923501.1:n.320-3423A>C
XR_001739749.1:n.331-29626A>C
XR_001739750.1:n.331-29626A>C
XR_001739751.1:n.331-29626A>C
XR_923501.2:n.331-3423A>C