Canonical Allele Identifier: CA2216768476
Gene: CTF2P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30904715G= , CM000678.2:g.30904715G= GRCh38
NC_000016.9:g.30916036G= , CM000678.1:g.30916036G= GRCh37
NC_000016.8:g.30823537G= NCBI36
NG_009171.1:g.13109G= , LRG_408:g.13109G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000412003.1:n.237C=