Canonical Allele Identifier: CA495783741
Gene: RBL2 HGNC NCBI

Linked Data

MyVariant Identifiers: chr16:g.53504729A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.53470817A>G , CM000678.2:g.53470817A>G GRCh38
NC_000016.9:g.53504729A>G , CM000678.1:g.53504729A>G GRCh37
NC_000016.8:g.52062230A>G NCBI36

Transcript Alleles

HGVS Amino-acid change
ENST00000262133.11:c.2598A>G MANE Select ENSP00000262133.6:p.Lys866=
ENST00000680543.1:n.4389A>G
ENST00000262133.10:c.2598A>G ENSP00000262133.6:p.Lys866=
ENST00000379935.8:n.2297A>G
ENST00000544545.2:c.1728A>G ENSP00000444685.2:p.Lys576=
NM_005611.3:c.2598A>G NP_005602.3:p.Lys866=
XM_005256083.3:c.2376A>G XP_005256140.1:p.Lys792=
XM_011523252.1:c.2598A>G XP_011521554.1:p.Lys866=
XM_011523253.1:c.1950A>G XP_011521555.1:p.Lys650=
NM_001323608.1:c.2598A>G NP_001310537.1:p.Lys866=
NM_001323609.1:c.2598A>G NP_001310538.1:p.Lys866=
NM_001323610.1:c.2451A>G NP_001310539.1:p.Lys817=
NM_001323611.1:c.2376A>G NP_001310540.1:p.Lys792=
XM_011523253.2:c.1950A>G XP_011521555.1:p.Lys650=
XM_017023513.1:c.1950A>G XP_016879002.1:p.Lys650=
NM_005611.4:c.2598A>G MANE Select NP_005602.3:p.Lys866=
NM_001323608.2:c.2598A>G NP_001310537.1:p.Lys866=
NM_001323609.2:c.2598A>G NP_001310538.1:p.Lys866=
NM_001323610.2:c.2451A>G NP_001310539.1:p.Lys817=