Canonical Allele Identifier: CA1033291368
Gene:

Linked Data

dbSNP Id: rs879746798
gnomAD v3: 2-88016319-C-G
gnomAD v4: 2-88016319-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016319C>G , CM000664.2:g.88016319C>G GRCh38
NC_000002.11:g.88315838C>G , CM000664.1:g.88315838C>G GRCh37
NC_000002.10:g.88096953C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.664C>G
XR_940336.3:n.664C>G