Canonical Allele Identifier: CA269464

Gene:

Linked Data

• ClinVar Variation Id: 126568
• ClinVar RCV Id: RCV001030427
• dbSNP Id: rs515726053
• gnomAD v2: 16-23614433-T-G
• gnomAD v3: 16-23603112-T-G
• gnomAD v4: 16-23603112-T-G
• MyVariant Identifiers: chr16:g.23614433T>G (hg19) ; chr16:g.23603112T>G (hg38)
• PubMed: PMID:21932393

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.23603112T>G , CM000678.2:g.23603112T>G	GRCh38
NC_000016.9:g.23614433T>G , CM000678.1:g.23614433T>G	GRCh37
NC_000016.8:g.23521934T>G	NCBI36
NG_007406.1:g.43246A>C , LRG_308:g.43246A>C