Canonical Allele Identifier: CA992978125
Gene: RPL36 HGNC NCBI

Linked Data

gnomAD v3: 19-5691456-A-T
gnomAD v4: 19-5691456-A-T

Genomic Alleles

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

Transcript Alleles

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