Canonical Allele Identifier: CA2799117969

Gene: RB1

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48348835T>C , CM000675.2:g.48348835T>C	GRCh38
NC_000013.10:g.48922971T>C , CM000675.1:g.48922971T>C	GRCh37
NC_000013.9:g.47820972T>C	NCBI36
NG_009009.1:g.50089T>C , LRG_517:g.50089T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.540-121T>C MANE Select	ENSP00000267163.4:n.540-121T>C
ENST00000650461.1:c.540-121T>C	ENSP00000497193.1:n.540-121T>C
ENST00000267163.4:c.540-121T>C	ENSP00000267163.4:n.540-121T>C
ENST00000467505.5:c.138-11182T>C	ENSP00000434702.1:n.138-11182T>C
ENST00000525036.1:n.702-121T>C
NM_000321.2:c.540-121T>C , LRG_517t1:c.540-121T>C	NP_000312.2:n.540-121T>C
XM_011535171.1:c.279-121T>C	XP_011533473.1:n.279-121T>C
XM_011535171.2:c.279-121T>C	XP_011533473.1:n.279-121T>C
NM_000321.3:c.540-121T>C MANE Select	NP_000312.2:n.540-121T>C