Canonical Allele Identifier: CA2185570236
Gene:

Linked Data

dbSNP Id: rs1895833422

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.69755851A>G , CM000677.2:g.69755851A>G GRCh38
NC_000015.9:g.70048190A>G , CM000677.1:g.70048190A>G GRCh37
NC_000015.8:g.67835244A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_001751592.2:n.86-305A>G