Canonical Allele Identifier: CA178436373

Gene:

Linked Data

• ClinVar Variation Id: 38800
• ClinVar RCV Id: RCV003894839
• dbSNP Id: rs12721510
• gnomAD v2: 8-67091182-G-T
• gnomAD v3: 8-66178947-G-T
• gnomAD v4: 8-66178947-G-T
• MyVariant Identifiers: chr8:g.67091182G>T (hg19) ; chr8:g.66178947G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000008.11:g.66178947G>T , CM000670.2:g.66178947G>T	GRCh38
NC_000008.10:g.67091182G>T , CM000670.1:g.67091182G>T	GRCh37
NC_000008.9:g.67253736G>T	NCBI36
NG_016127.1:g.4517C>A