Canonical Allele Identifier: CA445747779

Gene:

Linked Data

• ClinVar Variation Id: 469898
• ClinVar RCV Id: RCV003651967
• dbSNP Id: rs1554060095
• gnomAD v3: 5-112707339-A-T
• gnomAD v4: 5-112707339-A-T
• MyVariant Identifiers: chr5:g.112043036A>T (hg19) ; chr5:g.112707339A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707339A>T , CM000667.2:g.112707339A>T	GRCh38
NC_000005.9:g.112043036A>T , CM000667.1:g.112043036A>T	GRCh37
NC_000005.8:g.112070935A>T	NCBI36
NG_008481.4:g.19819A>T , LRG_130:g.19819A>T