Canonical Allele Identifier: CA494685589
Gene: CTF2P HGNC NCBI

Linked Data

dbSNP Id: rs1441724161
gnomAD v3: 16-30904717-C-T
gnomAD v4: 16-30904717-C-T
MyVariant Identifiers: chr16:g.30916038C>T (hg19) chr16:g.30904717C>T (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000412003.1:n.235G>A
Search 100 bp 5'
Search 100 bp 3'