Canonical Allele Identifier: CA2089971106
Gene: RB1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48380134G= , CM000675.2:g.48380134G= GRCh38
NC_000013.10:g.48954270G= , CM000675.1:g.48954270G= GRCh37
NC_000013.9:g.47852271G= NCBI36
NG_009009.1:g.81388G= , LRG_517:g.81388G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.1422-31G= MANE Select ENSP00000267163.4:n.1422-31G=
ENST00000650461.1:c.1422-31G= ENSP00000497193.1:n.1422-31G=
ENST00000267163.4:c.1422-31G= ENSP00000267163.4:n.1422-31G=
NM_000321.2:c.1422-31G= , LRG_517t1:c.1422-31G= NP_000312.2:n.1422-31G=
XM_011535171.1:c.1161-31G= XP_011533473.1:n.1161-31G=
XM_011535171.2:c.1161-31G= XP_011533473.1:n.1161-31G=
NM_000321.3:c.1422-31G= MANE Select NP_000312.2:n.1422-31G=
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