Canonical Allele Identifier: CA54680788

Gene:

Linked Data

• dbSNP Id: rs1015979531
• gnomAD v3: 2-120487268-A-G
• gnomAD v4: 2-120487268-A-G
• MyVariant Identifiers: chr2:g.121244844A>G (hg19) ; chr2:g.120487268A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.120487268A>G , CM000664.2:g.120487268A>G	GRCh38
NC_000002.11:g.121244844A>G , CM000664.1:g.121244844A>G	GRCh37
NC_000002.10:g.120961314A>G	NCBI36