Canonical Allele Identifier: CA2575413641
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48459603del , CM000675.2:g.48459603del GRCh38
NC_000013.10:g.49033739del , CM000675.1:g.49033739del GRCh37
NC_000013.9:g.47931740del NCBI36
NG_009009.1:g.160857del , LRG_517:g.160857del

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1961-85del MANE Select ENSP00000267163.4:n.1961-85del
ENST00000643064.1:c.194+78160del
ENST00000650461.1:c.1961-85del ENSP00000497193.1:n.1961-85del
ENST00000267163.4:c.1961-85del ENSP00000267163.4:n.1961-85del
NM_000321.2:c.1961-85del , LRG_517t1:c.1961-85del NP_000312.2:n.1961-85del
XM_011535171.1:c.1700-85del XP_011533473.1:n.1700-85del
XM_011535171.2:c.1700-85del XP_011533473.1:n.1700-85del
NM_000321.3:c.1961-85del MANE Select NP_000312.2:n.1961-85del