Canonical Allele Identifier: CA15653310
Gene:

Linked Data

dbSNP Id: rs17625382

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.57812948G>A , CM000672.2:g.57812948G>A GRCh38
NC_000010.10:g.59572708G>A , CM000672.1:g.59572708G>A GRCh37
NC_000010.9:g.59242714G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_945979.1:n.68+34344C>T
XR_001747454.1:n.85+34344C>T