Canonical Allele Identifier: CA645509200

Gene:

Linked Data

• ClinVar Variation Id: 439124
• ClinVar RCV Id: RCV000506005
• dbSNP Id: rs1555449252
• MyVariant Identifiers: chr16:g.222833C>G (hg19) ; chr16:g.172834C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.172834C>G , CM000678.2:g.172834C>G	GRCh38
NC_000016.9:g.222833C>G , CM000678.1:g.222833C>G	GRCh37
NC_000016.8:g.162833C>G	NCBI36
NG_000006.1:g.33697C>G
NG_059186.1:g.1184C>G
NG_059271.1:g.4988C>G