Canonical Allele Identifier: CA2024154288
Gene:

Linked Data

dbSNP Id: rs1865524847

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.28045351G>A , CM000674.2:g.28045351G>A GRCh38
NC_000012.11:g.28198284G>A , CM000674.1:g.28198284G>A GRCh37
NC_000012.10:g.28089551G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_931460.1:n.154-6393C>T