Canonical Allele Identifier: CA308568386

Gene: RPS19

Linked Data

• dbSNP Id: rs1366610
• gnomAD v3: 19-41869228-A-G
• gnomAD v4: 19-41869228-A-G
• MyVariant Identifiers: chr19:g.41869228A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.41869228A>G , CM000681.2:g.41869228A>G	GRCh38
NG_007080.3:g.14311A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000598742.6:c.356+14A>G MANE Select	ENSP00000470972.1:n.356+14A>G
ENST00000600467.6:c.356+14A>G	ENSP00000469228.2:n.356+14A>G
ENST00000221975.6:c.134+14A>G	ENSP00000221975.2:n.134+14A>G
ENST00000593863.5:c.356+14A>G	ENSP00000470004.1:n.356+14A>G
ENST00000598742.5:c.356+14A>G	ENSP00000470972.1:n.356+14A>G
NM_001022.3:c.356+14A>G	NP_001013.1:n.356+14A>G
NM_001321483.1:c.356+14A>G	NP_001308412.1:n.356+14A>G
NM_001321484.1:c.356+14A>G	NP_001308413.1:n.356+14A>G
NM_001321485.1:c.369+14A>G	NP_001308414.1:n.369+14A>G
XM_017027113.2:c.356+14A>G	XP_016882602.1:n.356+14A>G
NM_001022.4:c.356+14A>G MANE Select	NP_001013.1:n.356+14A>G
NM_001321483.2:c.356+14A>G	NP_001308412.1:n.356+14A>G
NM_001321484.2:c.356+14A>G	NP_001308413.1:n.356+14A>G
NM_001321485.2:c.369+14A>G	NP_001308414.1:n.369+14A>G