Canonical Allele Identifier: CA278115133

Gene:

Linked Data

• dbSNP Id: rs921774543
• gnomAD v2: 16-9343541-T-G
• gnomAD v3: 16-9249684-T-G
• gnomAD v4: 16-9249684-T-G
• MyVariant Identifiers: chr16:g.9343541T>G (hg19) ; chr16:g.9249684T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9249684T>G , CM000678.2:g.9249684T>G	GRCh38
NC_000016.9:g.9343541T>G , CM000678.1:g.9343541T>G	GRCh37
NC_000016.8:g.9251042T>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_933054.1:n.70+64951T>G