Canonical Allele Identifier: CA388250272

Gene: RB1

Linked Data

• gnomAD v4: 13-48303986-C-A
• MyVariant Identifiers: chr13:g.48878122C>A (hg19) ; chr13:g.48303986C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48303986C>A , CM000675.2:g.48303986C>A	GRCh38
NC_000013.10:g.48878122C>A , CM000675.1:g.48878122C>A	GRCh37
NC_000013.9:g.47776123C>A	NCBI36
NG_009009.1:g.5240C>A , LRG_517:g.5240C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.74C>A MANE Select	ENSP00000267163.4:p.Pro25Gln
ENST00000646097.1:c.74C>A	ENSP00000496556.1:p.Pro25Gln
ENST00000650461.1:c.74C>A	ENSP00000497193.1:p.Pro25Gln
ENST00000267163.4:c.74C>A	ENSP00000267163.4:p.Pro25Gln
ENST00000467505.5:c.74C>A	ENSP00000434702.1:p.Pro25Gln
ENST00000525036.1:n.236C>A
NM_000321.2:c.74C>A , LRG_517t1:c.74C>A	NP_000312.2:p.Pro25Gln
NM_000321.3:c.74C>A MANE Select	NP_000312.2:p.Pro25Gln