Canonical Allele Identifier: CA2206404280
Gene:

Linked Data

dbSNP Id: rs1265314248

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.9249697A>G , CM000678.2:g.9249697A>G GRCh38
NC_000016.9:g.9343554A>G , CM000678.1:g.9343554A>G GRCh37
NC_000016.8:g.9251055A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_933054.1:n.70+64964A>G