Canonical Allele Identifier: CA2089971102
Gene: RB1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48380129A= , CM000675.2:g.48380129A= GRCh38
NC_000013.10:g.48954265A= , CM000675.1:g.48954265A= GRCh37
NC_000013.9:g.47852266A= NCBI36
NG_009009.1:g.81383A= , LRG_517:g.81383A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.1422-36A= MANE Select ENSP00000267163.4:n.1422-36A=
ENST00000650461.1:c.1422-36A= ENSP00000497193.1:n.1422-36A=
ENST00000267163.4:c.1422-36A= ENSP00000267163.4:n.1422-36A=
NM_000321.2:c.1422-36A= , LRG_517t1:c.1422-36A= NP_000312.2:n.1422-36A=
XM_011535171.1:c.1161-36A= XP_011533473.1:n.1161-36A=
XM_011535171.2:c.1161-36A= XP_011533473.1:n.1161-36A=
NM_000321.3:c.1422-36A= MANE Select NP_000312.2:n.1422-36A=
Search 100 bp 5'
Search 100 bp 3'