Canonical Allele Identifier: CA134766643
Gene: OFCC1 HGNC NCBI

Linked Data

dbSNP Id: rs577800721
gnomAD v3: 6-10175609-G-C
gnomAD v4: 6-10175609-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10175609G>C , CM000668.2:g.10175609G>C GRCh38
NC_000006.11:g.10175842G>C , CM000668.1:g.10175842G>C GRCh37
NC_000006.10:g.10283828G>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000462111.1:n.164-16110C>G
ENST00000481704.1:c.-101-16110C>G ENSP00000418286.1:n.-101-16110C>G
XM_017011612.1:c.-101-16110C>G XP_016867101.1:n.-101-16110C>G
NR_170155.1:n.232-16110C>G