Canonical Allele Identifier: CA304045279
Gene: RPS15 HGNC NCBI

Linked Data

dbSNP Id: rs116840813
gnomAD v2: 19-1440136-A-G
gnomAD v4: 19-1440137-A-G
MyVariant Identifiers: chr19:g.1440136A>G (hg19) chr19:g.1440137A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.1440137A>G , CM000681.2:g.1440137A>G GRCh38
NC_000019.9:g.1440136A>G , CM000681.1:g.1440136A>G GRCh37
NC_000019.8:g.1391136A>G NCBI36
NG_017014.1:g.6774A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000592588.7:c.208A>G MANE Select ENSP00000467466.3:p.Met70Val
ENST00000233609.8:c.127A>G ENSP00000473953.1:p.Met43Val
ENST00000585665.2:c.109A>G ENSP00000466366.2:p.Met37Val
ENST00000586096.3:c.208A>G ENSP00000465055.2:p.Met70Val
ENST00000586656.5:c.109A>G ENSP00000475096.1:p.Met37Val
ENST00000586686.6:c.109A>G ENSP00000467676.2:p.Met37Val
ENST00000589656.6:c.208A>G ENSP00000467855.2:p.Met70Val
ENST00000591032.1:c.178A>G ENSP00000474970.2:p.Met60Val
ENST00000591804.6:c.109A>G ENSP00000474543.1:p.Met37Val
ENST00000592588.6:c.208A>G ENSP00000467466.3:p.Met70Val
ENST00000592623.5:c.127A>G ENSP00000474433.2:p.Met43Val
ENST00000592700.2:n.1340A>G
ENST00000593052.5:c.229A>G ENSP00000466010.1:p.Met77Val
NM_001018.3:c.208A>G NP_001009.1:p.Met70Val
NM_001018.4:c.208A>G NP_001009.1:p.Met70Val
NM_001308226.1:c.229A>G NP_001295155.1:p.Met77Val
NM_001018.5:c.208A>G MANE Select NP_001009.1:p.Met70Val
NM_001308226.2:c.229A>G NP_001295155.1:p.Met77Val
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