Canonical Allele Identifier: CA134766646
Gene: OFCC1 HGNC NCBI

Linked Data

dbSNP Id: rs974794573
gnomAD v3: 6-10175646-GT-G
gnomAD v4: 6-10175646-GT-G
MyVariant Identifiers: chr6:g.10175880del (hg19) chr6:g.10175647del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10175651del , CM000668.2:g.10175651del GRCh38
NC_000006.11:g.10175884del , CM000668.1:g.10175884del GRCh37
NC_000006.10:g.10283870del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000462111.1:n.164-16148del
ENST00000481704.1:c.-101-16148del ENSP00000418286.1:n.-101-16148del
XM_017011612.1:c.-101-16148del XP_016867101.1:n.-101-16148del
NR_170155.1:n.232-16148del
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