Canonical Allele Identifier: CA1609762398
Gene: OFCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1757821446

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.9993460A>G , CM000668.2:g.9993460A>G GRCh38
NC_000006.11:g.9993693A>G , CM000668.1:g.9993693A>G GRCh37
NC_000006.10:g.10101679A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000472329.5:n.117-54111T>C
ENST00000481704.1:c.6-54111T>C ENSP00000418286.1:n.6-54111T>C
ENST00000485268.1:c.-290-45998T>C ENSP00000417933.1:n.-290-45998T>C
XM_011515036.1:c.123-54111T>C XP_011513338.1:n.123-54111T>C
XM_017011612.1:c.6-54111T>C XP_016867101.1:n.6-54111T>C
NR_170155.1:n.338-54111T>C