Canonical Allele Identifier: CA51878250
Gene:

Linked Data

dbSNP Id: rs926027364
gnomAD v2: 2-88315531-T-G
gnomAD v3: 2-88016012-T-G
gnomAD v4: 2-88016012-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016012T>G , CM000664.2:g.88016012T>G GRCh38
NC_000002.11:g.88315531T>G , CM000664.1:g.88315531T>G GRCh37
NC_000002.10:g.88096646T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
XR_940335.3:n.357T>G
XR_940336.3:n.357T>G