Canonical Allele Identifier: CA483561097

Gene: RB1

Linked Data

• MyVariant Identifiers: chr13:g.49050938A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48476802A>G , CM000675.2:g.48476802A>G	GRCh38
NC_000013.10:g.49050938A>G , CM000675.1:g.49050938A>G	GRCh37
NC_000013.9:g.47948939A>G	NCBI36
NG_009009.1:g.178056A>G , LRG_517:g.178056A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2622A>G MANE Select	ENSP00000267163.4:p.Lys874=
ENST00000643064.1:c.194+95359A>G
ENST00000650461.1:c.2622A>G	ENSP00000497193.1:p.Lys874=
ENST00000267163.4:c.2622A>G	ENSP00000267163.4:p.Lys874=
ENST00000484879.1:n.356A>G
ENST00000531171.5:n.225A>G
NM_000321.2:c.2622A>G , LRG_517t1:c.2622A>G	NP_000312.2:p.Lys874=
XM_011535171.1:c.2361A>G	XP_011533473.1:p.Lys787=
XM_011535171.2:c.2361A>G	XP_011533473.1:p.Lys787=
NM_000321.3:c.2622A>G MANE Select	NP_000312.2:p.Lys874=