Canonical Allele Identifier: CA802056936

Gene:

Linked Data

• ClinVar Variation Id: 1371537
• ClinVar RCV Id: RCV003534762
• dbSNP Id: rs1312495728
• gnomAD v4: 5-112707457-T-G
• MyVariant Identifiers: chr5:g.112043154T>G (hg19) ; chr5:g.112707457T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707457T>G , CM000667.2:g.112707457T>G	GRCh38
NC_000005.9:g.112043154T>G , CM000667.1:g.112043154T>G	GRCh37
NC_000005.8:g.112071053T>G	NCBI36
NG_008481.4:g.19937T>G , LRG_130:g.19937T>G