Canonical Allele Identifier: CA2539015643
Gene: DDX39B HGNC NCBI
ATP6V1G2-DDX39B HGNC NCBI

Linked Data

gnomAD v4: 6-31533452-T-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.31533452T>G , CM000668.2:g.31533452T>G GRCh38
NC_000006.11:g.31501229T>G , CM000668.1:g.31501229T>G GRCh37
NC_000006.10:g.31609208T>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000396172.6:c.736-541A>C (DDX39B) MANE Select ENSP00000379475.1:n.736-541A>C
ENST00000376177.6:c.736-541A>C (DDX39B) ENSP00000365347.2:n.736-541A>C
ENST00000376185.5:c.*950-541A>C (ATP6V1G2-DDX39B) ENSP00000365356.1:n.*950-541A>C
ENST00000396172.5:c.736-541A>C (DDX39B) ENSP00000379475.1:n.736-541A>C
ENST00000417023.5:c.27-541A>C (DDX39B)
ENST00000427214.5:c.736-541A>C (DDX39B) ENSP00000399371.1:n.736-541A>C
ENST00000431908.5:c.502-541A>C (DDX39B) ENSP00000408000.1:n.502-541A>C
ENST00000458640.5:c.736-541A>C (DDX39B) ENSP00000416269.1:n.736-541A>C
ENST00000462256.5:n.2720A>C (DDX39B)
ENST00000481456.1:n.4119A>C (DDX39B)
ENST00000482195.5:n.969-541A>C (DDX39B)
ENST00000484566.5:c.110-541A>C (DDX39B)
NM_004640.6:c.736-541A>C (DDX39B) NP_004631.1:n.736-541A>C
NM_080598.5:c.736-541A>C (DDX39B) NP_542165.1:n.736-541A>C
NR_037852.1:n.1173-541A>C (DDX39B)
NR_037853.1:n.1539-541A>C (ATP6V1G2-DDX39B)
NM_004640.7:c.736-541A>C (DDX39B) MANE Select NP_004631.1:n.736-541A>C
NM_080598.6:c.736-541A>C (DDX39B) NP_542165.1:n.736-541A>C
NR_037852.2:n.701-541A>C (DDX39B)