Canonical Allele Identifier: CA395913817

Gene: RBL2

Linked Data

• gnomAD v4: 16-53470821-A-G
• MyVariant Identifiers: chr16:g.53504733A>G (hg19) ; chr16:g.53470821A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53470821A>G , CM000678.2:g.53470821A>G	GRCh38
NC_000016.9:g.53504733A>G , CM000678.1:g.53504733A>G	GRCh37
NC_000016.8:g.52062234A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262133.11:c.2602A>G MANE Select	ENSP00000262133.6:p.Ile868Val
ENST00000680543.1:n.4393A>G
ENST00000262133.10:c.2602A>G	ENSP00000262133.6:p.Ile868Val
ENST00000379935.8:n.2301A>G
ENST00000544545.2:c.1732A>G	ENSP00000444685.2:p.Ile578Val
NM_005611.3:c.2602A>G	NP_005602.3:p.Ile868Val
XM_005256083.3:c.2380A>G	XP_005256140.1:p.Ile794Val
XM_011523252.1:c.2602A>G	XP_011521554.1:p.Ile868Val
XM_011523253.1:c.1954A>G	XP_011521555.1:p.Ile652Val
NM_001323608.1:c.2602A>G	NP_001310537.1:p.Ile868Val
NM_001323609.1:c.2602A>G	NP_001310538.1:p.Ile868Val
NM_001323610.1:c.2455A>G	NP_001310539.1:p.Ile819Val
NM_001323611.1:c.2380A>G	NP_001310540.1:p.Ile794Val
XM_011523253.2:c.1954A>G	XP_011521555.1:p.Ile652Val
XM_017023513.1:c.1954A>G	XP_016879002.1:p.Ile652Val
NM_005611.4:c.2602A>G MANE Select	NP_005602.3:p.Ile868Val
NM_001323608.2:c.2602A>G	NP_001310537.1:p.Ile868Val
NM_001323609.2:c.2602A>G	NP_001310538.1:p.Ile868Val
NM_001323610.2:c.2455A>G	NP_001310539.1:p.Ile819Val