Canonical Allele Identifier: CA2022606248
Gene:

Linked Data

dbSNP Id: rs1954909214

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.24617922C>A , CM000674.2:g.24617922C>A GRCh38
NC_000012.11:g.24770856C>A , CM000674.1:g.24770856C>A GRCh37
NC_000012.10:g.24662123C>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749046.1:n.425-112G>T