Canonical Allele Identifier: CA2255111915
Gene:

Linked Data

dbSNP Id: rs1235242985

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237237T>G , CM000679.2:g.30237237T>G GRCh38
NC_000017.10:g.28564255T>G , CM000679.1:g.28564255T>G GRCh37
NC_000017.9:g.25588381T>G NCBI36
NG_011747.2:g.3700A>C

Transcript Alleles

HGVS Amino-acid change
XR_934654.1:n.165+167T>G
XR_001752824.1:n.280+167T>G