Canonical Allele Identifier: CA2573138733

Gene:

Linked Data

• ClinVar Variation Id: 1378003
• ClinVar RCV Id: RCV003772644
• dbSNP Id: rs2149627939

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.112707326A>T , CM000667.2:g.112707326A>T	GRCh38
NC_000005.9:g.112043023A>T , CM000667.1:g.112043023A>T	GRCh37
NC_000005.8:g.112070922A>T	NCBI36
NG_008481.4:g.19806A>T , LRG_130:g.19806A>T