Canonical Allele Identifier: CA388157474
Community Standard Title: NM_000321.3(RB1):c.2615T>C (p.Leu872Pro)
Gene: RB1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48476795T>C , CM000675.2:g.48476795T>C GRCh38
NC_000013.10:g.49050931T>C , CM000675.1:g.49050931T>C GRCh37
NC_000013.9:g.47948932T>C NCBI36
NG_009009.1:g.178049T>C , LRG_517:g.178049T>C

Transcript Alleles

HGVS Amino-acid Change
NM_000321.3:c.2615T>C MANE Select NP_000312.2:p.Leu872Pro
ENST00000267163.6:c.2615T>C MANE Select ENSP00000267163.4:p.Leu872Pro
NM_000321.2:c.2615T>C , LRG_517t1:c.2615T>C NP_000312.2:p.Leu872Pro
ENST00000267163.4:c.2615T>C ENSP00000267163.4:p.Leu872Pro
ENST00000484879.1:n.349T>C
ENST00000531171.5:n.218T>C
ENST00000643064.1:c.194+95352T>C
ENST00000650461.1:c.2615T>C ENSP00000497193.1:p.Leu872Pro
XM_011535171.1:c.2354T>C XP_011533473.1:p.Leu785Pro
XM_011535171.2:c.2354T>C XP_011533473.1:p.Leu785Pro