Canonical Allele Identifier: CA951207949
Gene:

Linked Data

dbSNP Id: rs1881755415

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.102501458G>A , CM000674.2:g.102501458G>A GRCh38
NC_000012.11:g.102895236G>A , CM000674.1:g.102895236G>A GRCh37
NC_000012.10:g.101419366G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749289.1:n.1952+17570G>A