Canonical Allele Identifier: CA268761542

Gene:

Linked Data

• ClinVar Variation Id: 1222480
• ClinVar RCV Id: RCV001598110
• dbSNP Id: rs28390245
• gnomAD v2: 15-40453058-G-T
• gnomAD v3: 15-40160857-G-T
• gnomAD v4: 15-40160857-G-T
• MyVariant Identifiers: chr15:g.40453058G>T (hg19) ; chr15:g.40160857G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.40160857G>T , CM000677.2:g.40160857G>T	GRCh38
NC_000015.9:g.40453058G>T , CM000677.1:g.40453058G>T	GRCh37
NC_000015.8:g.38240350G>T	NCBI36
NG_016338.1:g.4849G>T , LRG_489:g.4849G>T