Canonical Allele Identifier: CA10783892

Gene:

Linked Data

• ClinVar Variation Id: 1220560
• ClinVar RCV Id: RCV001595122
• dbSNP Id: rs235920
• gnomAD v2: 1-171621975-A-G
• gnomAD v3: 1-171652835-A-G
• gnomAD v4: 1-171652835-A-G
• MyVariant Identifiers: chr1:g.171621975A>G (hg19) ; chr1:g.171652835A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.171652835A>G , CM000663.2:g.171652835A>G	GRCh38
NC_000001.10:g.171621975A>G , CM000663.1:g.171621975A>G	GRCh37
NC_000001.9:g.169888598A>G	NCBI36
NG_008859.1:g.4799T>C