Canonical Allele Identifier: CA2624006087
Gene: OSGEP HGNC NCBI

Linked Data

gnomAD v4: 14-20454844-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20454844A>T , CM000676.2:g.20454844A>T GRCh38
NC_000014.8:g.20923003A>T , CM000676.1:g.20923003A>T GRCh37
NC_000014.7:g.19992843A>T NCBI36
NG_008718.1:g.4714A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000206542.8:c.-161T>A ENSP00000206542.4:n.-161T>A
ENST00000556252.1:n.210T>A
ENST00000556439.1:n.246T>A
NM_017807.3:c.-161T>A NP_060277.1:n.-161T>A
XM_011536930.1:c.-222T>A XP_011535232.1:n.-222T>A
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