Canonical Allele Identifier: CA403524081

Gene: RPL36

Linked Data

• gnomAD v4: 19-5691562-C-T
• MyVariant Identifiers: chr19:g.5691573C>T (hg19) ; chr19:g.5691562C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5691562C>T , CM000681.2:g.5691562C>T	GRCh38
NC_000019.9:g.5691573C>T , CM000681.1:g.5691573C>T	GRCh37
NC_000019.8:g.5642573C>T	NCBI36
NG_017015.1:g.6302C>T
NG_033142.1:g.33891G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000347512.8:c.259C>T MANE Select	ENSP00000252543.3:p.Arg87Trp
ENST00000347512.7:c.259C>T	ENSP00000252543.3:p.Arg87Trp
ENST00000394580.2:c.259C>T	ENSP00000378081.2:p.Arg87Trp
ENST00000577222.5:c.259C>T	ENSP00000464342.1:p.Arg87Trp
ENST00000579446.1:c.*52C>T	ENSP00000464613.1:n.*52C>T
ENST00000579649.5:c.259C>T	ENSP00000462609.1:p.Arg87Trp
NM_015414.3:c.259C>T	NP_056229.2:p.Arg87Trp
NM_033643.2:c.259C>T	NP_378669.1:p.Arg87Trp
NM_033643.3:c.259C>T MANE Select	NP_378669.1:p.Arg87Trp
NM_015414.4:c.259C>T	NP_056229.2:p.Arg87Trp