Canonical Allele Identifier: CA495783762

Gene: RBL2

Linked Data

• MyVariant Identifiers: chr16:g.53504747T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53470835T>C , CM000678.2:g.53470835T>C	GRCh38
NC_000016.9:g.53504747T>C , CM000678.1:g.53504747T>C	GRCh37
NC_000016.8:g.52062248T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid change
ENST00000262133.11:c.2616T>C MANE Select	ENSP00000262133.6:p.Phe872=
ENST00000680543.1:n.4407T>C
ENST00000262133.10:c.2616T>C	ENSP00000262133.6:p.Phe872=
ENST00000379935.8:n.2315T>C
ENST00000544545.2:c.1746T>C	ENSP00000444685.2:p.Phe582=
NM_005611.3:c.2616T>C	NP_005602.3:p.Phe872=
XM_005256083.3:c.2394T>C	XP_005256140.1:p.Phe798=
XM_011523252.1:c.2616T>C	XP_011521554.1:p.Phe872=
XM_011523253.1:c.1968T>C	XP_011521555.1:p.Phe656=
NM_001323608.1:c.2616T>C	NP_001310537.1:p.Phe872=
NM_001323609.1:c.2616T>C	NP_001310538.1:p.Phe872=
NM_001323610.1:c.2469T>C	NP_001310539.1:p.Phe823=
NM_001323611.1:c.2394T>C	NP_001310540.1:p.Phe798=
XM_011523253.2:c.1968T>C	XP_011521555.1:p.Phe656=
XM_017023513.1:c.1968T>C	XP_016879002.1:p.Phe656=
NM_005611.4:c.2616T>C MANE Select	NP_005602.3:p.Phe872=
NM_001323608.2:c.2616T>C	NP_001310537.1:p.Phe872=
NM_001323609.2:c.2616T>C	NP_001310538.1:p.Phe872=
NM_001323610.2:c.2469T>C	NP_001310539.1:p.Phe823=