Canonical Allele Identifier: CA494685566
Gene: CTF2P HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.30916030A>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30904709A>T , CM000678.2:g.30904709A>T GRCh38
NC_000016.9:g.30916030A>T , CM000678.1:g.30916030A>T GRCh37
NC_000016.8:g.30823531A>T NCBI36
NG_009171.1:g.13103A>T , LRG_408:g.13103A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000412003.1:n.243T>A
Search 100 bp 5'
Search 100 bp 3'