Canonical Allele Identifier: CA403524097

Gene: RPL36

Linked Data

• MyVariant Identifiers: chr19:g.5691580A>T (hg19) ; chr19:g.5691569A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5691569A>T , CM000681.2:g.5691569A>T	GRCh38
NC_000019.9:g.5691580A>T , CM000681.1:g.5691580A>T	GRCh37
NC_000019.8:g.5642580A>T	NCBI36
NG_017015.1:g.6309A>T
NG_033142.1:g.33884T>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000347512.8:c.266A>T MANE Select	ENSP00000252543.3:p.Glu89Val
ENST00000347512.7:c.266A>T	ENSP00000252543.3:p.Glu89Val
ENST00000394580.2:c.266A>T	ENSP00000378081.2:p.Glu89Val
ENST00000577222.5:c.266A>T	ENSP00000464342.1:p.Glu89Val
ENST00000579446.1:c.*59A>T	ENSP00000464613.1:n.*59A>T
ENST00000579649.5:c.266A>T	ENSP00000462609.1:p.Glu89Val
NM_015414.3:c.266A>T	NP_056229.2:p.Glu89Val
NM_033643.2:c.266A>T	NP_378669.1:p.Glu89Val
NM_033643.3:c.266A>T MANE Select	NP_378669.1:p.Glu89Val
NM_015414.4:c.266A>T	NP_056229.2:p.Glu89Val