Canonical Allele Identifier: CA2336668922
Gene: RPS19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41869205A= , CM000681.2:g.41869205A= GRCh38
NC_000019.9:g.42373275A= , CM000681.1:g.42373275A= GRCh37
NC_000019.8:g.47065115A= NCBI36
NG_007080.2:g.14288A=
NG_007080.3:g.14288A=

Transcript Alleles

HGVS Amino-acid change
ENST00000598742.6:c.347A= MANE Select ENSP00000470972.1:p.Asp116=
ENST00000600467.6:c.347A= ENSP00000469228.2:p.Asp116=
ENST00000221975.6:c.125A= ENSP00000221975.2:p.Asp42=
ENST00000593863.5:c.347A= ENSP00000470004.1:p.Asp116=
ENST00000598742.5:c.347A= ENSP00000470972.1:p.Asp116=
NM_001022.3:c.347A= NP_001013.1:p.Asp116=
NM_001321483.1:c.347A= NP_001308412.1:p.Asp116=
NM_001321484.1:c.347A= NP_001308413.1:p.Asp116=
NM_001321485.1:c.360A= NP_001308414.1:p.Gly120=
XM_017027113.2:c.347A= XP_016882602.1:p.Asp116=
NM_001022.4:c.347A= MANE Select NP_001013.1:p.Asp116=
NM_001321483.2:c.347A= NP_001308412.1:p.Asp116=
NM_001321484.2:c.347A= NP_001308413.1:p.Asp116=
NM_001321485.2:c.360A= NP_001308414.1:p.Gly120=