Canonical Allele Identifier: CA419447863

Gene: CYMP

Linked Data - Variant Effect Evidence

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.110491187T>A , CM000663.2:g.110491187T>A	GRCh38
NC_000001.10:g.111033809T>A , CM000663.1:g.111033809T>A	GRCh37
NC_000001.9:g.110835332T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000462836.2:n.555T>A
ENST00000420853.1:n.359T>A
ENST00000474680.5:n.1173T>A
NR_003599.2:n.1159T>A