Canonical Allele Identifier: CA2320057940
Gene: RPL36 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.5691456A= , CM000681.2:g.5691456A= GRCh38
NC_000019.9:g.5691467A= , CM000681.1:g.5691467A= GRCh37
NC_000019.8:g.5642467A= NCBI36
NG_017015.1:g.6196A=
NG_033142.1:g.33997T=

Transcript Alleles

HGVS Amino-acid change
ENST00000347512.8:c.228+3A= MANE Select ENSP00000252543.3:n.228+3A=
ENST00000347512.7:c.228+3A= ENSP00000252543.3:n.228+3A=
ENST00000394580.2:c.228+3A= ENSP00000378081.2:n.228+3A=
ENST00000577222.5:c.228+3A= ENSP00000464342.1:n.228+3A=
ENST00000579446.1:c.231A= ENSP00000464613.1:p.Val77=
ENST00000579649.5:c.228+3A= ENSP00000462609.1:n.228+3A=
NM_015414.3:c.228+3A= NP_056229.2:n.228+3A=
NM_033643.2:c.228+3A= NP_378669.1:n.228+3A=
NM_033643.3:c.228+3A= MANE Select NP_378669.1:n.228+3A=
NM_015414.4:c.228+3A= NP_056229.2:n.228+3A=