Canonical Allele Identifier: CA10587001

Gene:

Linked Data

• ClinVar Variation Id: 256215
• ClinVar RCV Id: RCV000250369 ; RCV001277066 ; RCV001532819 ; RCV001682980
• dbSNP Id: rs12386601
• gnomAD v2: 7-92157886-A-G
• gnomAD v3: 7-92528572-A-G
• gnomAD v4: 7-92528572-A-G
• MyVariant Identifiers: chr7:g.92157886A>G (hg19) ; chr7:g.92528572A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.92528572A>G , CM000669.2:g.92528572A>G	GRCh38
NC_000007.13:g.92157886A>G , CM000669.1:g.92157886A>G	GRCh37
NC_000007.12:g.91995822A>G	NCBI36
NG_008341.1:g.4960T>C
NG_008341.2:g.4960T>C