Canonical Allele Identifier: CA494685565
Gene: CTF2P HGNC NCBI

Linked Data

dbSNP Id: rs1297012019
gnomAD v3: 16-30904709-A-G
gnomAD v4: 16-30904709-A-G
MyVariant Identifiers: chr16:g.30916030A>G (hg19) chr16:g.30904709A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30904709A>G , CM000678.2:g.30904709A>G GRCh38
NC_000016.9:g.30916030A>G , CM000678.1:g.30916030A>G GRCh37
NC_000016.8:g.30823531A>G NCBI36
NG_009171.1:g.13103A>G , LRG_408:g.13103A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000412003.1:n.243T>C
Search 100 bp 5'
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