Canonical Allele Identifier: CA2090019424
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48459610_48459611delinsCG , CM000675.2:g.48459610_48459611delinsCG GRCh38
NC_000013.10:g.49033746_49033747delinsCG , CM000675.1:g.49033746_49033747delinsCG GRCh37
NC_000013.9:g.47931747_47931748delinsCG NCBI36
NG_009009.1:g.160864_160865delinsCG , LRG_517:g.160864_160865delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1961-78_1961-77delinsCG MANE Select ENSP00000267163.4:n.1961-78_1961-77delins...
ENST00000643064.1:c.194+78167_194+78168delinsCG
ENST00000650461.1:c.1961-78_1961-77delinsCG ENSP00000497193.1:n.1961-78_1961-77delins...
ENST00000267163.4:c.1961-78_1961-77delinsCG ENSP00000267163.4:n.1961-78_1961-77delins...
NM_000321.2:c.1961-78_1961-77delinsCG , LRG_517t1:c.1961-78_1961-77delinsCG NP_000312.2:n.1961-78_1961-77delinsCG
XM_011535171.1:c.1700-78_1700-77delinsCG XP_011533473.1:n.1700-78_1700-77delinsCG
XM_011535171.2:c.1700-78_1700-77delinsCG XP_011533473.1:n.1700-78_1700-77delinsCG
NM_000321.3:c.1961-78_1961-77delinsCG MANE Select NP_000312.2:n.1961-78_1961-77delinsCG