Canonical Allele Identifier: CA2700867495
Gene:

Linked Data

dbSNP Id: rs2105325248

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870182G>C , CM000664.2:g.155870182G>C GRCh38
NC_000002.11:g.156726694G>C , CM000664.1:g.156726694G>C GRCh37
NC_000002.10:g.156434940G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-2995C>G
XR_001739749.1:n.331-29198C>G
XR_001739750.1:n.331-29198C>G
XR_001739751.1:n.331-29198C>G
XR_923501.2:n.331-2995C>G