Canonical Allele Identifier: CA2336668919
Gene: RPS19 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41869196T= , CM000681.2:g.41869196T= GRCh38
NC_000019.9:g.42373266T= , CM000681.1:g.42373266T= GRCh37
NC_000019.8:g.47065106T= NCBI36
NG_007080.2:g.14279T=
NG_007080.3:g.14279T=

Transcript Alleles

HGVS Amino-acid change
ENST00000598742.6:c.338T= MANE Select ENSP00000470972.1:p.Val113=
ENST00000600467.6:c.338T= ENSP00000469228.2:p.Val113=
ENST00000221975.6:c.116T= ENSP00000221975.2:p.Val39=
ENST00000593863.5:c.338T= ENSP00000470004.1:p.Val113=
ENST00000598742.5:c.338T= ENSP00000470972.1:p.Val113=
NM_001022.3:c.338T= NP_001013.1:p.Val113=
NM_001321483.1:c.338T= NP_001308412.1:p.Val113=
NM_001321484.1:c.338T= NP_001308413.1:p.Val113=
NM_001321485.1:c.351T= NP_001308414.1:p.Gly117=
XM_017027113.2:c.338T= XP_016882602.1:p.Val113=
NM_001022.4:c.338T= MANE Select NP_001013.1:p.Val113=
NM_001321483.2:c.338T= NP_001308412.1:p.Val113=
NM_001321484.2:c.338T= NP_001308413.1:p.Val113=
NM_001321485.2:c.351T= NP_001308414.1:p.Gly117=