Canonical Allele Identifier: CA300346767

Gene:

Linked Data

• dbSNP Id: rs892526527
• MyVariant Identifiers: chr18:g.49001671C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.49001671C>T , CM000680.2:g.49001671C>T	GRCh38
NC_000018.9:g.46528041C>T , CM000680.1:g.46528041C>T	GRCh37
NC_000018.8:g.44782039C>T	NCBI36