Canonical Allele Identifier: CA658796584

Gene:

Linked Data

• ClinVar Variation Id: 537589
• ClinVar RCV Id: RCV000646547 ; RCV003892464
• dbSNP Id: rs1554060090
• gnomAD v3: 5-112707333-G-T
• gnomAD v4: 5-112707333-G-T
• MyVariant Identifiers: chr5:g.112043030G>T (hg19) ; chr5:g.112707333G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707333G>T , CM000667.2:g.112707333G>T	GRCh38
NC_000005.9:g.112043030G>T , CM000667.1:g.112043030G>T	GRCh37
NC_000005.8:g.112070929G>T	NCBI36
NG_008481.4:g.19813G>T , LRG_130:g.19813G>T