Canonical Allele Identifier: CA14265723
Gene: RBL2 HGNC NCBI

Linked Data

dbSNP Id: rs1074182

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.53437445T>G , CM000678.2:g.53437445T>G GRCh38
NC_000016.9:g.53471357T>G , CM000678.1:g.53471357T>G GRCh37
NC_000016.8:g.52028858T>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262133.11:c.241-1571T>G MANE Select ENSP00000262133.6:n.241-1571T>G
ENST00000680543.1:n.380-1571T>G
ENST00000262133.10:c.241-1571T>G ENSP00000262133.6:n.241-1571T>G
ENST00000544405.6:c.19-1571T>G ENSP00000443744.2:n.19-1571T>G
ENST00000567964.6:c.-153-1571T>G ENSP00000462464.1:n.-153-1571T>G
NM_005611.3:c.241-1571T>G NP_005602.3:n.241-1571T>G
XM_005256083.3:c.19-1571T>G XP_005256140.1:n.19-1571T>G
XM_011523252.1:c.241-1571T>G XP_011521554.1:n.241-1571T>G
NM_001323608.1:c.241-1571T>G NP_001310537.1:n.241-1571T>G
NM_001323609.1:c.241-1571T>G NP_001310538.1:n.241-1571T>G
NM_001323610.1:c.241-1571T>G NP_001310539.1:n.241-1571T>G
NM_001323611.1:c.19-1571T>G NP_001310540.1:n.19-1571T>G
NM_005611.4:c.241-1571T>G MANE Select NP_005602.3:n.241-1571T>G
NM_001323608.2:c.241-1571T>G NP_001310537.1:n.241-1571T>G
NM_001323609.2:c.241-1571T>G NP_001310538.1:n.241-1571T>G
NM_001323610.2:c.241-1571T>G NP_001310539.1:n.241-1571T>G