Canonical Allele Identifier: CA2216768479
Gene: CTF2P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30904717C= , CM000678.2:g.30904717C= GRCh38
NC_000016.9:g.30916038C= , CM000678.1:g.30916038C= GRCh37
NC_000016.8:g.30823539C= NCBI36
NG_009171.1:g.13111C= , LRG_408:g.13111C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000412003.1:n.235G=