Canonical Allele Identifier: CA2622985061
Gene: RB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48459588_48459589insATT , CM000675.2:g.48459588_48459589insATT GRCh38
NC_000013.10:g.49033724_49033725insATT , CM000675.1:g.49033724_49033725insATT GRCh37
NC_000013.9:g.47931725_47931726insATT NCBI36
NG_009009.1:g.160842_160843insATT , LRG_517:g.160842_160843insATT

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1961-100_1961-99insATT MANE Select ENSP00000267163.4:n.1961-100_1961-99insAT...
ENST00000643064.1:c.194+78145_194+78146insATT
ENST00000650461.1:c.1961-100_1961-99insATT ENSP00000497193.1:n.1961-100_1961-99insAT...
ENST00000267163.4:c.1961-100_1961-99insATT ENSP00000267163.4:n.1961-100_1961-99insAT...
NM_000321.2:c.1961-100_1961-99insATT , LRG_517t1:c.1961-100_1961-99insATT NP_000312.2:n.1961-100_1961-99insATT
XM_011535171.1:c.1700-100_1700-99insATT XP_011533473.1:n.1700-100_1700-99insATT
XM_011535171.2:c.1700-100_1700-99insATT XP_011533473.1:n.1700-100_1700-99insATT
NM_000321.3:c.1961-100_1961-99insATT MANE Select NP_000312.2:n.1961-100_1961-99insATT