Canonical Allele Identifier: CA494685579
Gene: CTF2P HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.30916035A>C (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30904714A>C , CM000678.2:g.30904714A>C GRCh38
NC_000016.9:g.30916035A>C , CM000678.1:g.30916035A>C GRCh37
NC_000016.8:g.30823536A>C NCBI36
NG_009171.1:g.13108A>C , LRG_408:g.13108A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000412003.1:n.238T>G
Search 100 bp 5'
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