Canonical Allele Identifier: CA494685573
Gene: CTF2P HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.30916033G>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30904712G>T , CM000678.2:g.30904712G>T GRCh38
NC_000016.9:g.30916033G>T , CM000678.1:g.30916033G>T GRCh37
NC_000016.8:g.30823534G>T NCBI36
NG_009171.1:g.13106G>T , LRG_408:g.13106G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000412003.1:n.240C>A
Search 100 bp 5'
Search 100 bp 3'