Canonical Allele Identifier: CA2840488098

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48349080A>C , CM000675.2:g.48349080A>C	GRCh38
NC_000013.10:g.48923216A>C , CM000675.1:g.48923216A>C	GRCh37
NC_000013.9:g.47821217A>C	NCBI36
NG_009009.1:g.50334A>C , LRG_517:g.50334A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.607+57A>C MANE Select	ENSP00000267163.4:n.607+57A>C
ENST00000650461.1:c.607+57A>C	ENSP00000497193.1:n.607+57A>C
ENST00000267163.4:c.607+57A>C	ENSP00000267163.4:n.607+57A>C
ENST00000467505.5:c.138-10937A>C	ENSP00000434702.1:n.138-10937A>C
ENST00000525036.1:n.769+57A>C
NM_000321.2:c.607+57A>C , LRG_517t1:c.607+57A>C	NP_000312.2:n.607+57A>C
XM_011535171.1:c.346+57A>C	XP_011533473.1:n.346+57A>C
XM_011535171.2:c.346+57A>C	XP_011533473.1:n.346+57A>C
NM_000321.3:c.607+57A>C MANE Select	NP_000312.2:n.607+57A>C