Canonical Allele Identifier: CA2089982342
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs1231786696
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48364871T>A , CM000675.2:g.48364871T>A GRCh38
NC_000013.10:g.48939007T>A , CM000675.1:g.48939007T>A GRCh37
NC_000013.9:g.47837008T>A NCBI36
NG_009009.1:g.66125T>A , LRG_517:g.66125T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.862-23T>A MANE Select ENSP00000267163.4:n.862-23T>A
ENST00000650461.1:c.862-23T>A ENSP00000497193.1:n.862-23T>A
ENST00000267163.4:c.862-23T>A ENSP00000267163.4:n.862-23T>A
NM_000321.2:c.862-23T>A , LRG_517t1:c.862-23T>A NP_000312.2:n.862-23T>A
XM_011535171.1:c.601-23T>A XP_011533473.1:n.601-23T>A
XM_011535171.2:c.601-23T>A XP_011533473.1:n.601-23T>A
NM_000321.3:c.862-23T>A MANE Select NP_000312.2:n.862-23T>A
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