Canonical Allele Identifier: CA494685562
Gene: CTF2P HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.30916029T>G (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30904708T>G , CM000678.2:g.30904708T>G GRCh38
NC_000016.9:g.30916029T>G , CM000678.1:g.30916029T>G GRCh37
NC_000016.8:g.30823530T>G NCBI36
NG_009171.1:g.13102T>G , LRG_408:g.13102T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000412003.1:n.244A>C
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