Canonical Allele Identifier: CA12180531
Gene: OFCC1 HGNC NCBI

Linked Data

dbSNP Id: rs116201121
gnomAD v2: 6-9993737-G-A
gnomAD v3: 6-9993504-G-A
gnomAD v4: 6-9993504-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.9993504G>A , CM000668.2:g.9993504G>A GRCh38
NC_000006.11:g.9993737G>A , CM000668.1:g.9993737G>A GRCh37
NC_000006.10:g.10101723G>A NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000472329.5:n.117-54155C>T
ENST00000481704.1:c.6-54155C>T ENSP00000418286.1:n.6-54155C>T
ENST00000485268.1:c.-290-46042C>T ENSP00000417933.1:n.-290-46042C>T
XM_011515036.1:c.123-54155C>T XP_011513338.1:n.123-54155C>T
XM_017011612.1:c.6-54155C>T XP_016867101.1:n.6-54155C>T
NR_170155.1:n.338-54155C>T