Canonical Allele Identifier: CA257404610
Gene: OSGEP HGNC NCBI

Linked Data

dbSNP Id: rs897879476
gnomAD v3: 14-20454878-C-T
gnomAD v4: 14-20454878-C-T
MyVariant Identifiers: chr14:g.20923037C>T (hg19) chr14:g.20454878C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20454878C>T , CM000676.2:g.20454878C>T GRCh38
NC_000014.8:g.20923037C>T , CM000676.1:g.20923037C>T GRCh37
NC_000014.7:g.19992877C>T NCBI36
NG_008718.1:g.4748C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000206542.8:c.-195G>A ENSP00000206542.4:n.-195G>A
ENST00000556252.1:n.176G>A
ENST00000556439.1:n.212G>A
NM_017807.3:c.-195G>A NP_060277.1:n.-195G>A
XM_011536930.1:c.-256G>A XP_011535232.1:n.-256G>A
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