Canonical Allele Identifier: CA494685572
Gene: CTF2P HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.30916032A>T (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30904711A>T , CM000678.2:g.30904711A>T GRCh38
NC_000016.9:g.30916032A>T , CM000678.1:g.30916032A>T GRCh37
NC_000016.8:g.30823533A>T NCBI36
NG_009171.1:g.13105A>T , LRG_408:g.13105A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000412003.1:n.241T>A
Search 100 bp 5'
Search 100 bp 3'