Canonical Allele Identifier: CA2090013958
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48452932A= , CM000675.2:g.48452932A= GRCh38
NC_000013.10:g.49027068A= , CM000675.1:g.49027068A= GRCh37
NC_000013.9:g.47925069A= NCBI36
NG_009009.1:g.154186A= , LRG_517:g.154186A=

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1696-61A= MANE Select ENSP00000267163.4:n.1696-61A=
ENST00000643064.1:c.194+71489A=
ENST00000650461.1:c.1696-61A= ENSP00000497193.1:n.1696-61A=
ENST00000267163.4:c.1696-61A= ENSP00000267163.4:n.1696-61A=
ENST00000480491.1:n.395-61A=
NM_000321.2:c.1696-61A= , LRG_517t1:c.1696-61A= NP_000312.2:n.1696-61A=
XM_011535171.1:c.1435-61A= XP_011533473.1:n.1435-61A=
XM_011535171.2:c.1435-61A= XP_011533473.1:n.1435-61A=
NM_000321.3:c.1696-61A= MANE Select NP_000312.2:n.1696-61A=