Canonical Allele Identifier: CA033440
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs562956970

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48459697T>A , CM000675.2:g.48459697T>A GRCh38
NC_000013.10:g.49033833T>A , CM000675.1:g.49033833T>A GRCh37
NC_000013.9:g.47931834T>A NCBI36
NG_009009.1:g.160951T>A , LRG_517:g.160951T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1970T>A MANE Select ENSP00000267163.4:p.Leu657Gln
ENST00000643064.1:c.194+78254T>A
ENST00000650461.1:c.1970T>A ENSP00000497193.1:p.Leu657Gln
ENST00000267163.4:c.1970T>A ENSP00000267163.4:p.Leu657Gln
NM_000321.2:c.1970T>A , LRG_517t1:c.1970T>A NP_000312.2:p.Leu657Gln
XM_011535171.1:c.1709T>A XP_011533473.1:p.Leu570Gln
XM_011535171.2:c.1709T>A XP_011533473.1:p.Leu570Gln
NM_000321.3:c.1970T>A MANE Select NP_000312.2:p.Leu657Gln