Canonical Allele Identifier: CA2024154251
Gene:

Linked Data

dbSNP Id: rs1865524106

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.28045254G>A , CM000674.2:g.28045254G>A GRCh38
NC_000012.11:g.28198187G>A , CM000674.1:g.28198187G>A GRCh37
NC_000012.10:g.28089454G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_931460.1:n.154-6296C>T