Canonical Allele Identifier: CA505179911

Gene: RPL36

Linked Data

• MyVariant Identifiers: chr19:g.5691575G>C (hg19)

Genomic Alleles

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

Transcript Alleles

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