Canonical Allele Identifier: CA982866920
Gene:

Linked Data

dbSNP Id: rs1597650504

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237411T>G , CM000679.2:g.30237411T>G GRCh38
NC_000017.10:g.28564429T>G , CM000679.1:g.28564429T>G GRCh37
NC_000017.9:g.25588555T>G NCBI36
NG_011747.2:g.3526A>C

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.166-231T>G
XR_001752824.1:n.281-231T>G