Canonical Allele Identifier: CA494685567
Gene: CTF2P HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.30916031A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30904710A>C , CM000678.2:g.30904710A>C GRCh38
NC_000016.9:g.30916031A>C , CM000678.1:g.30916031A>C GRCh37
NC_000016.8:g.30823532A>C NCBI36
NG_009171.1:g.13104A>C , LRG_408:g.13104A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000412003.1:n.242T>G
Search 100 bp 5'
Search 100 bp 3'