Canonical Allele Identifier: CA134766673
Gene: OFCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1008669349
gnomAD v3: 6-10175960-CT-C
gnomAD v4: 6-10175960-CT-C
MyVariant Identifiers: chr6:g.10176194del (hg19) chr6:g.10175961del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10175961del , CM000668.2:g.10175961del GRCh38
NC_000006.11:g.10176194del , CM000668.1:g.10176194del GRCh37
NC_000006.10:g.10284180del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000462111.1:n.164-16462del
ENST00000481704.1:c.-101-16462del ENSP00000418286.1:n.-101-16462del
XM_017011612.1:c.-101-16462del XP_016867101.1:n.-101-16462del
NR_170155.1:n.232-16462del
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