Canonical Allele Identifier: CA2573138749

Gene:

Linked Data

• ClinVar Variation Id: 1465398
• ClinVar RCV Id: RCV002569233
• dbSNP Id: rs1750554840

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707391A>T , CM000667.2:g.112707391A>T	GRCh38
NC_000005.9:g.112043088A>T , CM000667.1:g.112043088A>T	GRCh37
NC_000005.8:g.112070987A>T	NCBI36
NG_008481.4:g.19871A>T , LRG_130:g.19871A>T