Canonical Allele Identifier: CA2712969747
Gene:

Linked Data

dbSNP Id: rs2114577160

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.121837039G>A , CM000668.2:g.121837039G>A GRCh38
NC_000006.11:g.122158185G>A , CM000668.1:g.122158185G>A GRCh37
NC_000006.10:g.122199884G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_942936.1:n.241-20872G>A
XR_942937.1:n.240+69424G>A
XR_942938.1:n.241-20872G>A
XR_942939.1:n.241-20872G>A
XR_942940.1:n.241-20872G>A
XR_942941.1:n.241-20872G>A
XR_942936.2:n.241-20872G>A
XR_942937.3:n.240+69424G>A