Canonical Allele Identifier: CA278115131

Gene:

Linked Data

• dbSNP Id: rs546165538
• gnomAD v3: 16-9249668-C-G
• gnomAD v4: 16-9249668-C-G
• MyVariant Identifiers: chr16:g.9343525C>G (hg19) ; chr16:g.9249668C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.9249668C>G , CM000678.2:g.9249668C>G	GRCh38
NC_000016.9:g.9343525C>G , CM000678.1:g.9343525C>G	GRCh37
NC_000016.8:g.9251026C>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
XR_933054.1:n.70+64935C>G