Canonical Allele Identifier: CA406030603

Gene: RPS19

Linked Data

• dbSNP Id: rs1555841377
• gnomAD v2: 19-42373275-A-G
• gnomAD v4: 19-41869205-A-G
• MyVariant Identifiers: chr19:g.42373275A>G (hg19) ; chr19:g.41869205A>G (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000598742.6:c.347A>G MANE Select	ENSP00000470972.1:p.Asp116Gly
ENST00000600467.6:c.347A>G	ENSP00000469228.2:p.Asp116Gly
ENST00000221975.6:c.125A>G	ENSP00000221975.2:p.Asp42Gly
ENST00000593863.5:c.347A>G	ENSP00000470004.1:p.Asp116Gly
ENST00000598742.5:c.347A>G	ENSP00000470972.1:p.Asp116Gly
NM_001022.3:c.347A>G	NP_001013.1:p.Asp116Gly
NM_001321483.1:c.347A>G	NP_001308412.1:p.Asp116Gly
NM_001321484.1:c.347A>G	NP_001308413.1:p.Asp116Gly
NM_001321485.1:c.360A>G	NP_001308414.1:p.Gly120=
XM_017027113.2:c.347A>G	XP_016882602.1:p.Asp116Gly
NM_001022.4:c.347A>G MANE Select	NP_001013.1:p.Asp116Gly
NM_001321483.2:c.347A>G	NP_001308412.1:p.Asp116Gly
NM_001321484.2:c.347A>G	NP_001308413.1:p.Asp116Gly
NM_001321485.2:c.360A>G	NP_001308414.1:p.Gly120=