Canonical Allele Identifier: CA2728078249
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs2138358530

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48476624C>T , CM000675.2:g.48476624C>T GRCh38
NC_000013.10:g.49050760C>T , CM000675.1:g.49050760C>T GRCh37
NC_000013.9:g.47948761C>T NCBI36
NG_009009.1:g.177878C>T , LRG_517:g.177878C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.2521-77C>T MANE Select ENSP00000267163.4:n.2521-77C>T
ENST00000643064.1:c.194+95181C>T
ENST00000650461.1:c.2521-77C>T ENSP00000497193.1:n.2521-77C>T
ENST00000267163.4:c.2521-77C>T ENSP00000267163.4:n.2521-77C>T
ENST00000484879.1:n.178C>T
ENST00000531171.5:n.124-77C>T
NM_000321.2:c.2521-77C>T , LRG_517t1:c.2521-77C>T NP_000312.2:n.2521-77C>T
XM_011535171.1:c.2260-77C>T XP_011533473.1:n.2260-77C>T
XM_011535171.2:c.2260-77C>T XP_011533473.1:n.2260-77C>T
NM_000321.3:c.2521-77C>T MANE Select NP_000312.2:n.2521-77C>T