Canonical Allele Identifier: CA2255112077
Gene:

Linked Data

dbSNP Id: rs1597650503

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237409A>G , CM000679.2:g.30237409A>G GRCh38
NC_000017.10:g.28564427A>G , CM000679.1:g.28564427A>G GRCh37
NC_000017.9:g.25588553A>G NCBI36
NG_011747.2:g.3528T>C

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.166-233A>G
XR_001752824.1:n.281-233A>G