Canonical Allele Identifier: CA51878295
Gene:

Linked Data

dbSNP Id: rs561932884
gnomAD v3: 2-88016190-G-A
gnomAD v4: 2-88016190-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.88016190G>A , CM000664.2:g.88016190G>A GRCh38
NC_000002.11:g.88315709G>A , CM000664.1:g.88315709G>A GRCh37
NC_000002.10:g.88096824G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
XR_940335.3:n.535G>A
XR_940336.3:n.535G>A