Canonical Allele Identifier: CA1085896720
Gene: OFCC1 HGNC NCBI

Linked Data

dbSNP Id: rs1758339306
gnomAD v3: 6-10175647-T-A
gnomAD v4: 6-10175647-T-A
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.10175647T>A , CM000668.2:g.10175647T>A GRCh38
NC_000006.11:g.10175880T>A , CM000668.1:g.10175880T>A GRCh37
NC_000006.10:g.10283866T>A NCBI36

Transcript Alleles

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