Canonical Allele Identifier: CA2216768593
Gene: CTF2P HGNC NCBI

Linked Data

dbSNP Id: rs8046707
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Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.30904912G>C , CM000678.2:g.30904912G>C GRCh38
NC_000016.9:g.30916233G>C , CM000678.1:g.30916233G>C GRCh37
NC_000016.8:g.30823734G>C NCBI36
NG_009171.1:g.13306G>C , LRG_408:g.13306G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000412003.1:n.154-114C>G
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