Canonical Allele Identifier: CA495783748

Gene: RBL2

Linked Data

• MyVariant Identifiers: chr16:g.53504735C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53470823C>T , CM000678.2:g.53470823C>T	GRCh38
NC_000016.9:g.53504735C>T , CM000678.1:g.53504735C>T	GRCh37
NC_000016.8:g.52062236C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262133.11:c.2604C>T MANE Select	ENSP00000262133.6:p.Ile868=
ENST00000680543.1:n.4395C>T
ENST00000262133.10:c.2604C>T	ENSP00000262133.6:p.Ile868=
ENST00000379935.8:n.2303C>T
ENST00000544545.2:c.1734C>T	ENSP00000444685.2:p.Ile578=
NM_005611.3:c.2604C>T	NP_005602.3:p.Ile868=
XM_005256083.3:c.2382C>T	XP_005256140.1:p.Ile794=
XM_011523252.1:c.2604C>T	XP_011521554.1:p.Ile868=
XM_011523253.1:c.1956C>T	XP_011521555.1:p.Ile652=
NM_001323608.1:c.2604C>T	NP_001310537.1:p.Ile868=
NM_001323609.1:c.2604C>T	NP_001310538.1:p.Ile868=
NM_001323610.1:c.2457C>T	NP_001310539.1:p.Ile819=
NM_001323611.1:c.2382C>T	NP_001310540.1:p.Ile794=
XM_011523253.2:c.1956C>T	XP_011521555.1:p.Ile652=
XM_017023513.1:c.1956C>T	XP_016879002.1:p.Ile652=
NM_005611.4:c.2604C>T MANE Select	NP_005602.3:p.Ile868=
NM_001323608.2:c.2604C>T	NP_001310537.1:p.Ile868=
NM_001323609.2:c.2604C>T	NP_001310538.1:p.Ile868=
NM_001323610.2:c.2457C>T	NP_001310539.1:p.Ile819=