Canonical Allele Identifier: CA347658

Gene:

Linked Data

• ClinVar Variation Id: 217759
• ClinVar RCV Id: RCV000201837
• dbSNP Id: rs1611115
• gnomAD v2: 9-136500515-T-C
• gnomAD v3: 9-133635393-T-C
• gnomAD v4: 9-133635393-T-C
• MyVariant Identifiers: chr9:g.136500515T>C (hg19) ; chr9:g.133635393T>C (hg38)
• PubMed: PMID:20301647

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.133635393T>C , CM000671.2:g.133635393T>C	GRCh38
NC_000009.11:g.136500515T>C , CM000671.1:g.136500515T>C	GRCh37
NC_000009.10:g.135490336T>C	NCBI36
NG_008645.1:g.4031T>C