Canonical Allele Identifier: CA483557560

Gene: RB1

Linked Data

• MyVariant Identifiers: chr13:g.48923158A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48349022A>G , CM000675.2:g.48349022A>G	GRCh38
NC_000013.10:g.48923158A>G , CM000675.1:g.48923158A>G	GRCh37
NC_000013.9:g.47821159A>G	NCBI36
NG_009009.1:g.50276A>G , LRG_517:g.50276A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000267163.6:c.606A>G MANE Select	ENSP00000267163.4:p.Lys202=
ENST00000650461.1:c.606A>G	ENSP00000497193.1:p.Lys202=
ENST00000267163.4:c.606A>G	ENSP00000267163.4:p.Lys202=
ENST00000467505.5:c.138-10995A>G	ENSP00000434702.1:n.138-10995A>G
ENST00000525036.1:n.768A>G
NM_000321.2:c.606A>G , LRG_517t1:c.606A>G	NP_000312.2:p.Lys202=
XM_011535171.1:c.345A>G	XP_011533473.1:p.Lys115=
XM_011535171.2:c.345A>G	XP_011533473.1:p.Lys115=
NM_000321.3:c.606A>G MANE Select	NP_000312.2:p.Lys202=