Canonical Allele Identifier: CA10654513

Gene:

Linked Data

• ClinVar Variation Id: 369084
• ClinVar RCV Id: RCV000320378
• dbSNP Id: rs877081
• gnomAD v2: 14-94843083-G-A
• gnomAD v3: 14-94376746-G-A
• gnomAD v4: 14-94376746-G-A
• MyVariant Identifiers: chr14:g.94843083G>A (hg19) ; chr14:g.94376746G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000014.9:g.94376746G>A , CM000676.2:g.94376746G>A	GRCh38
NC_000014.8:g.94843083G>A , CM000676.1:g.94843083G>A	GRCh37
NC_000014.7:g.93912836G>A	NCBI36
NG_008290.1:g.18947C>T