Canonical Allele Identifier: CA2223143640
Gene: RBL2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.53470711T= , CM000678.2:g.53470711T= GRCh38
NC_000016.9:g.53504623T= , CM000678.1:g.53504623T= GRCh37
NC_000016.8:g.52062124T= NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262133.11:c.2527-35T= MANE Select ENSP00000262133.6:n.2527-35T=
ENST00000680543.1:n.4318-35T=
ENST00000262133.10:c.2527-35T= ENSP00000262133.6:n.2527-35T=
ENST00000379935.8:n.2226-35T=
ENST00000544545.2:c.1657-35T= ENSP00000444685.2:n.1657-35T=
NM_005611.3:c.2527-35T= NP_005602.3:n.2527-35T=
XM_005256083.3:c.2305-35T= XP_005256140.1:n.2305-35T=
XM_011523252.1:c.2527-35T= XP_011521554.1:n.2527-35T=
XM_011523253.1:c.1879-35T= XP_011521555.1:n.1879-35T=
NM_001323608.1:c.2527-35T= NP_001310537.1:n.2527-35T=
NM_001323609.1:c.2527-35T= NP_001310538.1:n.2527-35T=
NM_001323610.1:c.2380-35T= NP_001310539.1:n.2380-35T=
NM_001323611.1:c.2305-35T= NP_001310540.1:n.2305-35T=
XM_011523253.2:c.1879-35T= XP_011521555.1:n.1879-35T=
XM_017023513.1:c.1879-35T= XP_016879002.1:n.1879-35T=
NM_005611.4:c.2527-35T= MANE Select NP_005602.3:n.2527-35T=
NM_001323608.2:c.2527-35T= NP_001310537.1:n.2527-35T=
NM_001323609.2:c.2527-35T= NP_001310538.1:n.2527-35T=
NM_001323610.2:c.2380-35T= NP_001310539.1:n.2380-35T=