Canonical Allele Identifier: CA1905920025
Gene:

Linked Data

dbSNP Id: rs1297619354

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.43318673G>A , CM000672.2:g.43318673G>A GRCh38
NC_000010.10:g.43814121G>A , CM000672.1:g.43814121G>A GRCh37
NC_000010.9:g.43134127G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_945902.1:n.108+78G>A
XR_945902.2:n.198+78G>A