Canonical Allele Identifier: CA2122037937
Gene: OSGEP HGNC NCBI

Linked Data

dbSNP Id: rs1566511328

Genomic Alleles

HGVS Genome Assembly
NC_000014.9:g.20454815G>C , CM000676.2:g.20454815G>C GRCh38
NC_000014.8:g.20922974G>C , CM000676.1:g.20922974G>C GRCh37
NC_000014.7:g.19992814G>C NCBI36
NG_008718.1:g.4685G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000206542.8:c.-132C>G ENSP00000206542.4:n.-132C>G
ENST00000556252.1:n.239C>G
ENST00000556439.1:n.275C>G
NM_017807.3:c.-132C>G NP_060277.1:n.-132C>G
XM_011536930.1:c.-193C>G XP_011535232.1:n.-193C>G
XM_011536931.1:c.-428C>G XP_011535233.1:n.-428C>G