Canonical Allele Identifier: CA483559642

Gene: RB1

Linked Data

• MyVariant Identifiers: chr13:g.48955546A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48381410A>G , CM000675.2:g.48381410A>G	GRCh38
NC_000013.10:g.48955546A>G , CM000675.1:g.48955546A>G	GRCh37
NC_000013.9:g.47853547A>G	NCBI36
NG_009009.1:g.82664A>G , LRG_517:g.82664A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000267163.6:c.1662A>G MANE Select	ENSP00000267163.4:p.Glu554=
ENST00000643064.1:c.161A>G
ENST00000650461.1:c.1662A>G	ENSP00000497193.1:p.Glu554=
ENST00000267163.4:c.1662A>G	ENSP00000267163.4:p.Glu554=
NM_000321.2:c.1662A>G , LRG_517t1:c.1662A>G	NP_000312.2:p.Glu554=
XM_011535171.1:c.1401A>G	XP_011533473.1:p.Glu467=
XM_011535171.2:c.1401A>G	XP_011533473.1:p.Glu467=
NM_000321.3:c.1662A>G MANE Select	NP_000312.2:p.Glu554=