Canonical Allele Identifier: CA1085896730
Gene: OFCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1758339781
gnomAD v3: 6-10175693-G-A
gnomAD v4: 6-10175693-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10175693G>A , CM000668.2:g.10175693G>A GRCh38
NC_000006.11:g.10175926G>A , CM000668.1:g.10175926G>A GRCh37
NC_000006.10:g.10283912G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000462111.1:n.164-16194C>T
ENST00000481704.1:c.-101-16194C>T ENSP00000418286.1:n.-101-16194C>T
XM_017011612.1:c.-101-16194C>T XP_016867101.1:n.-101-16194C>T
NR_170155.1:n.232-16194C>T