Canonical Allele Identifier: CA10654695

Gene:

Linked Data

• ClinVar Variation Id: 369514
• ClinVar RCV Id: RCV000273887 ; RCV000319599 ; RCV004544720
• dbSNP Id: rs1800948
• gnomAD v2: 6-132129152-G-C
• gnomAD v3: 6-131808012-G-C
• gnomAD v4: 6-131808012-G-C
• MyVariant Identifiers: chr6:g.132129152G>C (hg19) ; chr6:g.131808012G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131808012G>C , CM000668.2:g.131808012G>C	GRCh38
NC_000006.11:g.132129152G>C , CM000668.1:g.132129152G>C	GRCh37
NC_000006.10:g.132170845G>C	NCBI36
NG_008206.1:g.4997G>C