Canonical Allele Identifier: CA403523912

Gene: RPL36

Linked Data

• MyVariant Identifiers: chr19:g.5691471G>C (hg19) ; chr19:g.5691460G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5691460G>C , CM000681.2:g.5691460G>C	GRCh38
NC_000019.9:g.5691471G>C , CM000681.1:g.5691471G>C	GRCh37
NC_000019.8:g.5642471G>C	NCBI36
NG_017015.1:g.6200G>C
NG_033142.1:g.33993C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000347512.8:c.228+7G>C MANE Select	ENSP00000252543.3:n.228+7G>C
ENST00000347512.7:c.228+7G>C	ENSP00000252543.3:n.228+7G>C
ENST00000394580.2:c.228+7G>C	ENSP00000378081.2:n.228+7G>C
ENST00000577222.5:c.228+7G>C	ENSP00000464342.1:n.228+7G>C
ENST00000579446.1:c.235G>C	ENSP00000464613.1:p.Gly79Arg
ENST00000579649.5:c.228+7G>C	ENSP00000462609.1:n.228+7G>C
NM_015414.3:c.228+7G>C	NP_056229.2:n.228+7G>C
NM_033643.2:c.228+7G>C	NP_378669.1:n.228+7G>C
NM_033643.3:c.228+7G>C MANE Select	NP_378669.1:n.228+7G>C
NM_015414.4:c.228+7G>C	NP_056229.2:n.228+7G>C