Canonical Allele Identifier: CA10577886

Gene:

Linked Data

• ClinVar Variation Id: 230210
• ClinVar RCV Id: RCV000214721
• dbSNP Id: rs763096037
• gnomAD v3: 2-47402930-G-T
• gnomAD v4: 2-47402930-G-T
• MyVariant Identifiers: chr2:g.47630069G>T (hg19) ; chr2:g.47402930G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.47402930G>T , CM000664.2:g.47402930G>T	GRCh38
NC_000002.11:g.47630069G>T , CM000664.1:g.47630069G>T	GRCh37
NC_000002.10:g.47483573G>T	NCBI36
NG_007110.2:g.4807G>T , LRG_218:g.4807G>T