Canonical Allele Identifier: CA2739274966

Gene:

Linked Data

• ClinVar Variation Id: 2786929
• ClinVar RCV Id: RCV003745742

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707410G>T , CM000667.2:g.112707410G>T	GRCh38
NC_000005.9:g.112043107G>T , CM000667.1:g.112043107G>T	GRCh37
NC_000005.8:g.112071006G>T	NCBI36
NG_008481.4:g.19890G>T , LRG_130:g.19890G>T