Canonical Allele Identifier: CA1140042689
Gene: CYMP HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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