Canonical Allele Identifier: CA494685590
Gene: CTF2P HGNC NCBI

Linked Data

gnomAD v4: 16-30904717-C-A
MyVariant Identifiers: chr16:g.30916038C>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30904717C>A , CM000678.2:g.30904717C>A GRCh38
NC_000016.9:g.30916038C>A , CM000678.1:g.30916038C>A GRCh37
NC_000016.8:g.30823539C>A NCBI36
NG_009171.1:g.13111C>A , LRG_408:g.13111C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000412003.1:n.235G>T
Search 100 bp 5'
Search 100 bp 3'