Canonical Allele Identifier: CA658655866

Gene:

Linked Data

• ClinVar Variation Id: 469900
• ClinVar RCV Id: RCV003651968
• dbSNP Id: rs1554060092
• MyVariant Identifiers: chr5:g.112043033A>T (hg19) ; chr5:g.112707336A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707336A>T , CM000667.2:g.112707336A>T	GRCh38
NC_000005.9:g.112043033A>T , CM000667.1:g.112043033A>T	GRCh37
NC_000005.8:g.112070932A>T	NCBI36
NG_008481.4:g.19816A>T , LRG_130:g.19816A>T