Canonical Allele Identifier: CA494685570
Gene: CTF2P HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.30916032A>C (hg19)
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Genomic Alleles

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

Transcript Alleles

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