Canonical Allele Identifier: CA1033291466

Gene:

Linked Data

• dbSNP Id: rs1172652497
• gnomAD v3: 2-88016337-T-G
• gnomAD v4: 2-88016337-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016337T>G , CM000664.2:g.88016337T>G	GRCh38
NC_000002.11:g.88315856T>G , CM000664.1:g.88315856T>G	GRCh37
NC_000002.10:g.88096971T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.682T>G
XR_940336.3:n.682T>G