Canonical Allele Identifier: CA2216768480
Gene: CTF2P HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30904718G= , CM000678.2:g.30904718G= GRCh38
NC_000016.9:g.30916039G= , CM000678.1:g.30916039G= GRCh37
NC_000016.8:g.30823540G= NCBI36
NG_009171.1:g.13112G= , LRG_408:g.13112G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000412003.1:n.234C=