Canonical Allele Identifier: CA1846127750

Gene:

Linked Data

• ClinVar Variation Id: 1978225
• ClinVar RCV Id: RCV002775007
• dbSNP Id: rs1171316483
• gnomAD v4: 9-35658059-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.35658059G>T , CM000671.2:g.35658059G>T	GRCh38
NC_000009.11:g.35658056G>T , CM000671.1:g.35658056G>T	GRCh37
NC_000009.10:g.35648056G>T	NCBI36
NG_017041.1:g.4960C>A , LRG_163:g.4960C>A
NG_033120.1:g.4770G>T