Canonical Allele Identifier: CA388250194
Gene: RB1 HGNC NCBI

Linked Data

MyVariant Identifiers: chr13:g.48878082A>C (hg19) chr13:g.48303946A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48303946A>C , CM000675.2:g.48303946A>C GRCh38
NC_000013.10:g.48878082A>C , CM000675.1:g.48878082A>C GRCh37
NC_000013.9:g.47776083A>C NCBI36
NG_009009.1:g.5200A>C , LRG_517:g.5200A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.34A>C MANE Select ENSP00000267163.4:p.Thr12Pro
ENST00000646097.1:c.34A>C ENSP00000496556.1:p.Thr12Pro
ENST00000650461.1:c.34A>C ENSP00000497193.1:p.Thr12Pro
ENST00000267163.4:c.34A>C ENSP00000267163.4:p.Thr12Pro
ENST00000467505.5:c.34A>C ENSP00000434702.1:p.Thr12Pro
ENST00000525036.1:n.196A>C
NM_000321.2:c.34A>C , LRG_517t1:c.34A>C NP_000312.2:p.Thr12Pro
NM_000321.3:c.34A>C MANE Select NP_000312.2:p.Thr12Pro
Search 100 bp 5'
Search 100 bp 3'