Canonical Allele Identifier: CA2624006167
Gene: OSGEP HGNC NCBI

Linked Data

gnomAD v4: 14-20454901-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20454901A>G , CM000676.2:g.20454901A>G GRCh38
NC_000014.8:g.20923060A>G , CM000676.1:g.20923060A>G GRCh37
NC_000014.7:g.19992900A>G NCBI36
NG_008718.1:g.4771A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000206542.8:c.-218T>C ENSP00000206542.4:n.-218T>C
ENST00000556252.1:n.153T>C
ENST00000556439.1:n.189T>C
NM_017807.3:c.-218T>C NP_060277.1:n.-218T>C
XM_011536930.1:c.-279T>C XP_011535232.1:n.-279T>C
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