Canonical Allele Identifier: CA11044149

Gene:

Linked Data

• ClinVar Variation Id: 1275378
• ClinVar RCV Id: RCV001679617
• dbSNP Id: rs114860453
• gnomAD v2: 2-215674619-G-C
• gnomAD v3: 2-214809895-G-C
• gnomAD v4: 2-214809895-G-C
• MyVariant Identifiers: chr2:g.215674619G>C (hg19) ; chr2:g.214809895G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.214809895G>C , CM000664.2:g.214809895G>C	GRCh38
NC_000002.11:g.215674619G>C , CM000664.1:g.215674619G>C	GRCh37
NC_000002.10:g.215382864G>C	NCBI36
NG_012047.2:g.4810C>G
NG_012047.3:g.4817C>G