Canonical Allele Identifier: CA304607182

Gene: RPL36

Linked Data

• dbSNP Id: rs1021449338
• gnomAD v2: 19-5691575-G-A
• gnomAD v3: 19-5691564-G-A
• gnomAD v4: 19-5691564-G-A
• MyVariant Identifiers: chr19:g.5691575G>A (hg19) ; chr19:g.5691564G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5691564G>A , CM000681.2:g.5691564G>A	GRCh38
NC_000019.9:g.5691575G>A , CM000681.1:g.5691575G>A	GRCh37
NC_000019.8:g.5642575G>A	NCBI36
NG_017015.1:g.6304G>A
NG_033142.1:g.33889C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000347512.8:c.261G>A MANE Select	ENSP00000252543.3:p.Arg87=
ENST00000347512.7:c.261G>A	ENSP00000252543.3:p.Arg87=
ENST00000394580.2:c.261G>A	ENSP00000378081.2:p.Arg87=
ENST00000577222.5:c.261G>A	ENSP00000464342.1:p.Arg87=
ENST00000579446.1:c.*54G>A	ENSP00000464613.1:n.*54G>A
ENST00000579649.5:c.261G>A	ENSP00000462609.1:p.Arg87=
NM_015414.3:c.261G>A	NP_056229.2:p.Arg87=
NM_033643.2:c.261G>A	NP_378669.1:p.Arg87=
NM_033643.3:c.261G>A MANE Select	NP_378669.1:p.Arg87=
NM_015414.4:c.261G>A	NP_056229.2:p.Arg87=