Canonical Allele Identifier: CA982866768
Gene:

Linked Data

dbSNP Id: rs1907327882

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.30237350C>G , CM000679.2:g.30237350C>G GRCh38
NC_000017.10:g.28564368C>G , CM000679.1:g.28564368C>G GRCh37
NC_000017.9:g.25588494C>G NCBI36
NG_011747.2:g.3587G>C

Transcript Alleles

HGVS Amino-acid Change
XR_934654.1:n.165+280C>G
XR_001752824.1:n.280+280C>G