Canonical Allele Identifier: CA150691036
Gene:

Linked Data

dbSNP Id: rs943013832

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.155817502G>A , CM000668.2:g.155817502G>A GRCh38
NC_000006.11:g.156138636G>A , CM000668.1:g.156138636G>A GRCh37
NC_000006.10:g.156180328G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_943142.1:n.79+24083G>A
XR_943146.1:n.552-2832C>T
XR_001744423.1:n.606-2832C>T
XR_001744424.1:n.79+24083G>A