Canonical Allele Identifier: CA494685575
Gene: CTF2P HGNC NCBI

Linked Data

gnomAD v4: 16-30904712-G-A
MyVariant Identifiers: chr16:g.30916033G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30904712G>A , CM000678.2:g.30904712G>A GRCh38
NC_000016.9:g.30916033G>A , CM000678.1:g.30916033G>A GRCh37
NC_000016.8:g.30823534G>A NCBI36
NG_009171.1:g.13106G>A , LRG_408:g.13106G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000412003.1:n.240C>T
Search 100 bp 5'
Search 100 bp 3'