Canonical Allele Identifier: CA565469901
Gene: OFCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1183905412
gnomAD v2: 6-10176187-C-CA
gnomAD v3: 6-10175954-C-CA
gnomAD v4: 6-10175954-C-CA
MyVariant Identifiers: chr6:g.10176187_10176188insA (hg19) chr6:g.10175954_10175955insA (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10175955dup , CM000668.2:g.10175955dup GRCh38
NC_000006.11:g.10176188dup , CM000668.1:g.10176188dup GRCh37
NC_000006.10:g.10284174dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000462111.1:n.164-16456dup
ENST00000481704.1:c.-101-16456dup ENSP00000418286.1:n.-101-16456dup
XM_017011612.1:c.-101-16456dup XP_016867101.1:n.-101-16456dup
NR_170155.1:n.232-16456dup
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