Canonical Allele Identifier: CA2700867491
Gene:

Linked Data

dbSNP Id: rs2105325243

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870179A>G , CM000664.2:g.155870179A>G GRCh38
NC_000002.11:g.156726691A>G , CM000664.1:g.156726691A>G GRCh37
NC_000002.10:g.156434937A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-2992T>C
XR_001739749.1:n.331-29195T>C
XR_001739750.1:n.331-29195T>C
XR_001739751.1:n.331-29195T>C
XR_923501.2:n.331-2992T>C