Canonical Allele Identifier: CA406030358
Gene: RPS19 HGNC NCBI

Linked Data

dbSNP Id: rs74678920

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.41869122G>A , CM000681.2:g.41869122G>A GRCh38
NC_000019.9:g.42373192G>A , CM000681.1:g.42373192G>A GRCh37
NC_000019.8:g.47065032G>A NCBI36
NG_007080.2:g.14205G>A
NG_007080.3:g.14205G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000598261.2:c.277G>A ENSP00000469798.1:p.Ala93Thr
ENST00000598742.6:c.264G>A MANE Select ENSP00000470972.1:p.Met88Ile
ENST00000600467.6:c.264G>A ENSP00000469228.2:p.Met88Ile
ENST00000221975.6:c.42G>A ENSP00000221975.2:p.Met14Ile
ENST00000593863.5:c.264G>A ENSP00000470004.1:p.Met88Ile
ENST00000598261.1:c.277G>A ENSP00000469798.1:p.Ala93Thr
ENST00000598399.1:c.1102G>A ENSP00000472660.1:n.1102G>A
ENST00000598742.5:c.264G>A ENSP00000470972.1:p.Met88Ile
NM_001022.3:c.264G>A NP_001013.1:p.Met88Ile
NM_001321483.1:c.264G>A NP_001308412.1:p.Met88Ile
NM_001321484.1:c.264G>A NP_001308413.1:p.Met88Ile
NM_001321485.1:c.277G>A NP_001308414.1:p.Ala93Thr
XM_017027113.2:c.264G>A XP_016882602.1:p.Met88Ile
NM_001022.4:c.264G>A MANE Select NP_001013.1:p.Met88Ile
NM_001321483.2:c.264G>A NP_001308412.1:p.Met88Ile
NM_001321484.2:c.264G>A NP_001308413.1:p.Met88Ile
NM_001321485.2:c.277G>A NP_001308414.1:p.Ala93Thr