Canonical Allele Identifier: CA2575413506
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48380140T>C , CM000675.2:g.48380140T>C GRCh38
NC_000013.10:g.48954276T>C , CM000675.1:g.48954276T>C GRCh37
NC_000013.9:g.47852277T>C NCBI36
NG_009009.1:g.81394T>C , LRG_517:g.81394T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.1422-25T>C MANE Select ENSP00000267163.4:n.1422-25T>C
ENST00000650461.1:c.1422-25T>C ENSP00000497193.1:n.1422-25T>C
ENST00000267163.4:c.1422-25T>C ENSP00000267163.4:n.1422-25T>C
NM_000321.2:c.1422-25T>C , LRG_517t1:c.1422-25T>C NP_000312.2:n.1422-25T>C
XM_011535171.1:c.1161-25T>C XP_011533473.1:n.1161-25T>C
XM_011535171.2:c.1161-25T>C XP_011533473.1:n.1161-25T>C
NM_000321.3:c.1422-25T>C MANE Select NP_000312.2:n.1422-25T>C