Canonical Allele Identifier: CA278115102

Gene:

Linked Data

• dbSNP Id: rs891111687
• gnomAD v3: 16-9249443-G-A
• gnomAD v4: 16-9249443-G-A
• MyVariant Identifiers: chr16:g.9343300G>A (hg19) ; chr16:g.9249443G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9249443G>A , CM000678.2:g.9249443G>A	GRCh38
NC_000016.9:g.9343300G>A , CM000678.1:g.9343300G>A	GRCh37
NC_000016.8:g.9250801G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_933054.1:n.70+64710G>A