Canonical Allele Identifier: CA1033291454

Gene:

Linked Data

• dbSNP Id: rs900315154
• gnomAD v3: 2-88016333-C-G
• gnomAD v4: 2-88016333-C-G

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.88016333C>G , CM000664.2:g.88016333C>G	GRCh38
NC_000002.11:g.88315852C>G , CM000664.1:g.88315852C>G	GRCh37
NC_000002.10:g.88096967C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_940335.3:n.678C>G
XR_940336.3:n.678C>G