Canonical Allele Identifier: CA9113818

Gene: RPL36

Linked Data

• dbSNP Id: rs753482460
• ExAC: 19:5691470 T / A
• gnomAD v2: 19-5691470-T-A
• gnomAD v4: 19-5691459-T-A
• MyVariant Identifiers: chr19:g.5691470T>A (hg19) ; chr19:g.5691459T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.5691459T>A , CM000681.2:g.5691459T>A	GRCh38
NC_000019.9:g.5691470T>A , CM000681.1:g.5691470T>A	GRCh37
NC_000019.8:g.5642470T>A	NCBI36
NG_017015.1:g.6199T>A
NG_033142.1:g.33994A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000347512.8:c.228+6T>A MANE Select	ENSP00000252543.3:n.228+6T>A
ENST00000347512.7:c.228+6T>A	ENSP00000252543.3:n.228+6T>A
ENST00000394580.2:c.228+6T>A	ENSP00000378081.2:n.228+6T>A
ENST00000577222.5:c.228+6T>A	ENSP00000464342.1:n.228+6T>A
ENST00000579446.1:c.234T>A	ENSP00000464613.1:p.Gly78=
ENST00000579649.5:c.228+6T>A	ENSP00000462609.1:n.228+6T>A
NM_015414.3:c.228+6T>A	NP_056229.2:n.228+6T>A
NM_033643.2:c.228+6T>A	NP_378669.1:n.228+6T>A
NM_033643.3:c.228+6T>A MANE Select	NP_378669.1:n.228+6T>A
NM_015414.4:c.228+6T>A	NP_056229.2:n.228+6T>A