Canonical Allele Identifier: CA2216768470
Gene: CTF2P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30904708T= , CM000678.2:g.30904708T= GRCh38
NC_000016.9:g.30916029T= , CM000678.1:g.30916029T= GRCh37
NC_000016.8:g.30823530T= NCBI36
NG_009171.1:g.13102T= , LRG_408:g.13102T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000412003.1:n.244A=