Canonical Allele Identifier: CA5045897
Gene:

Linked Data

ClinVar Variation Id: 2168092
ClinVar RCV Id: RCV003092819
dbSNP Id: rs145463993
ExAC: 9:35658046 T / G
gnomAD v2: 9-35658046-T-G
gnomAD v3: 9-35658049-T-G
gnomAD v4: 9-35658049-T-G
MyVariant Identifiers: chr9:g.35658046T>G (hg19) chr9:g.35658049T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.35658049T>G , CM000671.2:g.35658049T>G GRCh38
NC_000009.11:g.35658046T>G , CM000671.1:g.35658046T>G GRCh37
NC_000009.10:g.35648046T>G NCBI36
NG_017041.1:g.4970A>C , LRG_163:g.4970A>C
NG_033120.1:g.4760T>G
Search 100 bp 5'
Search 100 bp 3'