Canonical Allele Identifier: CA2090013932
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs1949336532
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48452895A>C , CM000675.2:g.48452895A>C GRCh38
NC_000013.10:g.49027031A>C , CM000675.1:g.49027031A>C GRCh37
NC_000013.9:g.47925032A>C NCBI36
NG_009009.1:g.154149A>C , LRG_517:g.154149A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1696-98A>C MANE Select ENSP00000267163.4:n.1696-98A>C
ENST00000643064.1:c.194+71452A>C
ENST00000650461.1:c.1696-98A>C ENSP00000497193.1:n.1696-98A>C
ENST00000267163.4:c.1696-98A>C ENSP00000267163.4:n.1696-98A>C
ENST00000480491.1:n.395-98A>C
NM_000321.2:c.1696-98A>C , LRG_517t1:c.1696-98A>C NP_000312.2:n.1696-98A>C
XM_011535171.1:c.1435-98A>C XP_011533473.1:n.1435-98A>C
XM_011535171.2:c.1435-98A>C XP_011533473.1:n.1435-98A>C
NM_000321.3:c.1696-98A>C MANE Select NP_000312.2:n.1696-98A>C
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