Canonical Allele Identifier: CA2622986200

Gene: RB1

Linked Data

• gnomAD v4: 13-48476971-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48476971C>A , CM000675.2:g.48476971C>A	GRCh38
NC_000013.10:g.49051107C>A , CM000675.1:g.49051107C>A	GRCh37
NC_000013.9:g.47949108C>A	NCBI36
NG_009009.1:g.178225C>A , LRG_517:g.178225C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.2663+128C>A MANE Select	ENSP00000267163.4:n.2663+128C>A
ENST00000643064.1:c.194+95528C>A
ENST00000650461.1:c.2663+128C>A	ENSP00000497193.1:n.2663+128C>A
ENST00000267163.4:c.2663+128C>A	ENSP00000267163.4:n.2663+128C>A
ENST00000484879.1:n.397+128C>A
ENST00000531171.5:n.266+128C>A
NM_000321.2:c.2663+128C>A , LRG_517t1:c.2663+128C>A	NP_000312.2:n.2663+128C>A
XM_011535171.1:c.2402+128C>A	XP_011533473.1:n.2402+128C>A
XM_011535171.2:c.2402+128C>A	XP_011533473.1:n.2402+128C>A
NM_000321.3:c.2663+128C>A MANE Select	NP_000312.2:n.2663+128C>A