Canonical Allele Identifier: CA1300258631
Gene:

Linked Data

dbSNP Id: rs570150282

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.155870230G>A , CM000664.2:g.155870230G>A GRCh38
NC_000002.11:g.156726742G>A , CM000664.1:g.156726742G>A GRCh37
NC_000002.10:g.156434988G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_923501.1:n.320-3043C>T
XR_001739749.1:n.331-29246C>T
XR_001739750.1:n.331-29246C>T
XR_001739751.1:n.331-29246C>T
XR_923501.2:n.331-3043C>T