Canonical Allele Identifier: CA2697549460

Gene:

Linked Data

• ClinVar Variation Id: 2681969
• ClinVar RCV Id: RCV003477261

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.172843C>T , CM000678.2:g.172843C>T	GRCh38
NC_000016.9:g.222842C>T , CM000678.1:g.222842C>T	GRCh37
NC_000016.8:g.162842C>T	NCBI36
NG_000006.1:g.33706C>T
NG_059186.1:g.1193C>T
NG_059271.1:g.4997C>T