Canonical Allele Identifier: CA395913848

Gene: RBL2

Linked Data

• MyVariant Identifiers: chr16:g.53504746T>A (hg19) ; chr16:g.53470834T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53470834T>A , CM000678.2:g.53470834T>A	GRCh38
NC_000016.9:g.53504746T>A , CM000678.1:g.53504746T>A	GRCh37
NC_000016.8:g.52062247T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262133.11:c.2615T>A MANE Select	ENSP00000262133.6:p.Phe872Tyr
ENST00000680543.1:n.4406T>A
ENST00000262133.10:c.2615T>A	ENSP00000262133.6:p.Phe872Tyr
ENST00000379935.8:n.2314T>A
ENST00000544545.2:c.1745T>A	ENSP00000444685.2:p.Phe582Tyr
NM_005611.3:c.2615T>A	NP_005602.3:p.Phe872Tyr
XM_005256083.3:c.2393T>A	XP_005256140.1:p.Phe798Tyr
XM_011523252.1:c.2615T>A	XP_011521554.1:p.Phe872Tyr
XM_011523253.1:c.1967T>A	XP_011521555.1:p.Phe656Tyr
NM_001323608.1:c.2615T>A	NP_001310537.1:p.Phe872Tyr
NM_001323609.1:c.2615T>A	NP_001310538.1:p.Phe872Tyr
NM_001323610.1:c.2468T>A	NP_001310539.1:p.Phe823Tyr
NM_001323611.1:c.2393T>A	NP_001310540.1:p.Phe798Tyr
XM_011523253.2:c.1967T>A	XP_011521555.1:p.Phe656Tyr
XM_017023513.1:c.1967T>A	XP_016879002.1:p.Phe656Tyr
NM_005611.4:c.2615T>A MANE Select	NP_005602.3:p.Phe872Tyr
NM_001323608.2:c.2615T>A	NP_001310537.1:p.Phe872Tyr
NM_001323609.2:c.2615T>A	NP_001310538.1:p.Phe872Tyr
NM_001323610.2:c.2468T>A	NP_001310539.1:p.Phe823Tyr