Canonical Allele Identifier: CA2370108
Gene: DHX30 HGNC NCBI

Linked Data

dbSNP Id: rs755074414
gnomAD v2: 3-47889722-G-A
gnomAD v3: 3-47848232-G-A
gnomAD v4: 3-47848232-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.47848232G>A , CM000665.2:g.47848232G>A GRCh38
NC_000003.11:g.47889722G>A , CM000665.1:g.47889722G>A GRCh37
NC_000003.10:g.47864726G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000445061.6:c.2339G>A MANE Select ENSP00000405620.1:p.Arg780Gln
ENST00000348968.8:c.2255G>A ENSP00000343442.4:p.Arg752Gln
ENST00000395745.6:c.*2239G>A ENSP00000379094.2:n.*2239G>A
ENST00000445061.5:c.2339G>A ENSP00000405620.1:p.Arg780Gln
ENST00000446256.6:c.2339G>A ENSP00000392601.3:p.Arg780Gln
ENST00000457607.1:c.2423G>A ENSP00000394682.1:p.Arg808Gln
ENST00000474183.1:n.456G>A
ENST00000619982.4:c.2222G>A ENSP00000483160.1:p.Arg741Gln
NM_014966.3:c.2222G>A NP_055781.2:p.Arg741Gln
NM_138615.2:c.2339G>A NP_619520.1:p.Arg780Gln
XM_006713033.1:c.2243G>A XP_006713096.1:p.Arg748Gln
XM_011533490.1:c.2552G>A XP_011531792.1:p.Arg851Gln
XM_011533491.1:c.2552G>A XP_011531793.1:p.Arg851Gln
XM_011533492.1:c.2552G>A XP_011531794.1:p.Arg851Gln
XM_011533493.1:c.2441G>A XP_011531795.1:p.Arg814Gln
XM_011533494.1:c.2339G>A XP_011531796.1:p.Arg780Gln
XM_011533495.1:c.2339G>A XP_011531797.1:p.Arg780Gln
XM_011533496.1:c.2255G>A XP_011531798.1:p.Arg752Gln
XM_011533497.1:c.2255G>A XP_011531799.1:p.Arg752Gln
XM_011533498.1:c.2255G>A XP_011531800.1:p.Arg752Gln
NM_001330990.1:c.2255G>A NP_001317919.1:p.Arg752Gln
XM_011533490.2:c.2552G>A XP_011531792.1:p.Arg851Gln
XM_011533494.3:c.2339G>A XP_011531796.1:p.Arg780Gln
XM_011533495.2:c.2339G>A XP_011531797.1:p.Arg780Gln
XM_011533497.2:c.2255G>A XP_011531799.1:p.Arg752Gln
XM_017005914.1:c.2471G>A XP_016861403.1:p.Arg824Gln
XM_017005915.1:c.2243G>A XP_016861404.1:p.Arg748Gln
XM_017005916.2:c.2228G>A XP_016861405.1:p.Arg743Gln
XM_017005917.1:c.2222G>A XP_016861406.1:p.Arg741Gln
XM_024453405.1:c.2441G>A XP_024309173.1:p.Arg814Gln
NM_138615.3:c.2339G>A MANE Select NP_619520.1:p.Arg780Gln
NM_001330990.2:c.2255G>A NP_001317919.1:p.Arg752Gln
NM_014966.4:c.2222G>A NP_055781.2:p.Arg741Gln