Canonical Allele Identifier: CA13956595
Gene:

Linked Data

ClinVar Variation Id: 1167989
ClinVar RCV Id: RCV001517840
dbSNP Id: rs2233406
gnomAD v2: 14-35874799-G-A
gnomAD v3: 14-35405593-G-A
gnomAD v4: 14-35405593-G-A
MyVariant Identifiers: chr14:g.35874799G>A (hg19) chr14:g.35405593G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.35405593G>A , CM000676.2:g.35405593G>A GRCh38
NC_000014.8:g.35874799G>A , CM000676.1:g.35874799G>A GRCh37
NC_000014.7:g.34944550G>A NCBI36
NG_007571.1:g.4146C>T , LRG_89:g.4146C>T
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