Canonical Allele Identifier: CA2720592090
Gene:

Linked Data

dbSNP Id: rs2119114430

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.129576808G>A , CM000671.2:g.129576808G>A GRCh38
NC_000009.11:g.132339087G>A , CM000671.1:g.132339087G>A GRCh37
NC_000009.10:g.131378908G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_930390.1:n.182+1210G>A