Canonical Allele Identifier: CA2622978369
Gene: RB1 HGNC NCBI

Linked Data

gnomAD v4: 13-48342526-A-G
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48342526A>G , CM000675.2:g.48342526A>G GRCh38
NC_000013.10:g.48916662A>G , CM000675.1:g.48916662A>G GRCh37
NC_000013.9:g.47814663A>G NCBI36
NG_009009.1:g.43780A>G , LRG_517:g.43780A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.265-73A>G MANE Select ENSP00000267163.4:n.265-73A>G
ENST00000650461.1:c.265-73A>G ENSP00000497193.1:n.265-73A>G
ENST00000267163.4:c.265-73A>G ENSP00000267163.4:n.265-73A>G
ENST00000467505.5:c.138-17491A>G ENSP00000434702.1:n.138-17491A>G
ENST00000525036.1:n.427-73A>G
NM_000321.2:c.265-73A>G , LRG_517t1:c.265-73A>G NP_000312.2:n.265-73A>G
XM_011535171.1:c.4-73A>G XP_011533473.1:n.4-73A>G
XM_011535171.2:c.4-73A>G XP_011533473.1:n.4-73A>G
NM_000321.3:c.265-73A>G MANE Select NP_000312.2:n.265-73A>G
Search 100 bp 5'
Search 100 bp 3'