Canonical Allele Identifier: CA388157005

Gene: RB1

Linked Data

• MyVariant Identifiers: chr13:g.48923153G>A (hg19) ; chr13:g.48349017G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48349017G>A , CM000675.2:g.48349017G>A	GRCh38
NC_000013.10:g.48923153G>A , CM000675.1:g.48923153G>A	GRCh37
NC_000013.9:g.47821154G>A	NCBI36
NG_009009.1:g.50271G>A , LRG_517:g.50271G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.601G>A MANE Select	ENSP00000267163.4:p.Ala201Thr
ENST00000650461.1:c.601G>A	ENSP00000497193.1:p.Ala201Thr
ENST00000267163.4:c.601G>A	ENSP00000267163.4:p.Ala201Thr
ENST00000467505.5:c.138-11000G>A	ENSP00000434702.1:n.138-11000G>A
ENST00000525036.1:n.763G>A
NM_000321.2:c.601G>A , LRG_517t1:c.601G>A	NP_000312.2:p.Ala201Thr
XM_011535171.1:c.340G>A	XP_011533473.1:p.Ala114Thr
XM_011535171.2:c.340G>A	XP_011533473.1:p.Ala114Thr
NM_000321.3:c.601G>A MANE Select	NP_000312.2:p.Ala201Thr