Canonical Allele Identifier: CA1033291189

Gene:

Linked Data

• gnomAD v3: 2-88016278-A-T
• gnomAD v4: 2-88016278-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016278A>T , CM000664.2:g.88016278A>T	GRCh38
NC_000002.11:g.88315797A>T , CM000664.1:g.88315797A>T	GRCh37
NC_000002.10:g.88096912A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.623A>T
XR_940336.3:n.623A>T