Canonical Allele Identifier: CA2499225376

Gene:

Linked Data

• ClinVar Variation Id: 1163126
• ClinVar RCV Id: RCV001507933
• dbSNP Id: rs2145930043
• gnomAD v4: 19-12887263-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.12887263G>A , CM000681.2:g.12887263G>A	GRCh38
NC_000019.9:g.12998077G>A , CM000681.1:g.12998077G>A	GRCh37
NC_000019.8:g.12859077G>A	NCBI36
NG_009292.1:g.1104G>A
NG_013087.1:g.4941C>T