Canonical Allele Identifier: CA2622980176
Gene: RB1 HGNC NCBI

Linked Data

gnomAD v4: 13-48364990-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48364990T>C , CM000675.2:g.48364990T>C GRCh38
NC_000013.10:g.48939126T>C , CM000675.1:g.48939126T>C GRCh37
NC_000013.9:g.47837127T>C NCBI36
NG_009009.1:g.66244T>C , LRG_517:g.66244T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.939+19T>C MANE Select ENSP00000267163.4:n.939+19T>C
ENST00000650461.1:c.939+19T>C ENSP00000497193.1:n.939+19T>C
ENST00000267163.4:c.939+19T>C ENSP00000267163.4:n.939+19T>C
NM_000321.2:c.939+19T>C , LRG_517t1:c.939+19T>C NP_000312.2:n.939+19T>C
XM_011535171.1:c.678+19T>C XP_011533473.1:n.678+19T>C
XM_011535171.2:c.678+19T>C XP_011533473.1:n.678+19T>C
XR_002957522.1:n.122-14A>G
NM_000321.3:c.939+19T>C MANE Select NP_000312.2:n.939+19T>C
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