Canonical Allele Identifier: CA949956431
Gene:

Linked Data

dbSNP Id: rs1872958141

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.84170223A>C , CM000674.2:g.84170223A>C GRCh38
NC_000012.11:g.84564002A>C , CM000674.1:g.84564002A>C GRCh37
NC_000012.10:g.83088133A>C NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_001749234.1:n.127+16243T>G
XR_001749235.1:n.127+16243T>G