Canonical Allele Identifier: CA271505085

Gene:

Linked Data

• ClinVar Variation Id: 1283010
• ClinVar RCV Id: RCV001689269
• dbSNP Id: rs28583784
• gnomAD v2: 15-65322166-C-A
• gnomAD v3: 15-65029828-C-A
• gnomAD v4: 15-65029828-C-A
• MyVariant Identifiers: chr15:g.65322166C>A (hg19) ; chr15:g.65322166_65322170delinsATTTA (hg19) ; chr15:g.65029828C>A (hg38) ; chr15:g.65029828_65029832delinsATTTA (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.65029828C>A , CM000677.2:g.65029828C>A	GRCh38
NC_000015.9:g.65322166C>A , CM000677.1:g.65322166C>A	GRCh37
NC_000015.8:g.63109219C>A	NCBI36
NG_029184.1:g.4812G>T