Canonical Allele Identifier: CA2700867518
Gene:

Linked Data

dbSNP Id: rs2105325264

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870207T>C , CM000664.2:g.155870207T>C GRCh38
NC_000002.11:g.156726719T>C , CM000664.1:g.156726719T>C GRCh37
NC_000002.10:g.156434965T>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3020A>G
XR_001739749.1:n.331-29223A>G
XR_001739750.1:n.331-29223A>G
XR_001739751.1:n.331-29223A>G
XR_923501.2:n.331-3020A>G