Canonical Allele Identifier: CA142276774

Gene:

Linked Data

• ClinVar Variation Id: 1271069
• ClinVar RCV Id: RCV001680590
• dbSNP Id: rs3812148
• gnomAD v2: 6-80816145-G-A
• gnomAD v3: 6-80106428-G-A
• gnomAD v4: 6-80106428-G-A
• MyVariant Identifiers: chr6:g.80816145G>A (hg19) ; chr6:g.80106428G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.80106428G>A , CM000668.2:g.80106428G>A	GRCh38
NC_000006.11:g.80816145G>A , CM000668.1:g.80816145G>A	GRCh37
NC_000006.10:g.80872864G>A	NCBI36
NG_009775.1:g.4802G>A
NG_009775.2:g.4802G>A