Canonical Allele Identifier: CA395913831

Gene: RBL2

Linked Data

• MyVariant Identifiers: chr16:g.53504739A>C (hg19) ; chr16:g.53470827A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.53470827A>C , CM000678.2:g.53470827A>C	GRCh38
NC_000016.9:g.53504739A>C , CM000678.1:g.53504739A>C	GRCh37
NC_000016.8:g.52062240A>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000262133.11:c.2608A>C MANE Select	ENSP00000262133.6:p.Thr870Pro
ENST00000680543.1:n.4399A>C
ENST00000262133.10:c.2608A>C	ENSP00000262133.6:p.Thr870Pro
ENST00000379935.8:n.2307A>C
ENST00000544545.2:c.1738A>C	ENSP00000444685.2:p.Thr580Pro
NM_005611.3:c.2608A>C	NP_005602.3:p.Thr870Pro
XM_005256083.3:c.2386A>C	XP_005256140.1:p.Thr796Pro
XM_011523252.1:c.2608A>C	XP_011521554.1:p.Thr870Pro
XM_011523253.1:c.1960A>C	XP_011521555.1:p.Thr654Pro
NM_001323608.1:c.2608A>C	NP_001310537.1:p.Thr870Pro
NM_001323609.1:c.2608A>C	NP_001310538.1:p.Thr870Pro
NM_001323610.1:c.2461A>C	NP_001310539.1:p.Thr821Pro
NM_001323611.1:c.2386A>C	NP_001310540.1:p.Thr796Pro
XM_011523253.2:c.1960A>C	XP_011521555.1:p.Thr654Pro
XM_017023513.1:c.1960A>C	XP_016879002.1:p.Thr654Pro
NM_005611.4:c.2608A>C MANE Select	NP_005602.3:p.Thr870Pro
NM_001323608.2:c.2608A>C	NP_001310537.1:p.Thr870Pro
NM_001323609.2:c.2608A>C	NP_001310538.1:p.Thr870Pro
NM_001323610.2:c.2461A>C	NP_001310539.1:p.Thr821Pro