Canonical Allele Identifier: CA483558975
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs2138335827
MyVariant Identifiers: chr13:g.49033832C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48459696C>T , CM000675.2:g.48459696C>T GRCh38
NC_000013.10:g.49033832C>T , CM000675.1:g.49033832C>T GRCh37
NC_000013.9:g.47931833C>T NCBI36
NG_009009.1:g.160950C>T , LRG_517:g.160950C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1969C>T MANE Select ENSP00000267163.4:p.Leu657=
ENST00000643064.1:c.194+78253C>T
ENST00000650461.1:c.1969C>T ENSP00000497193.1:p.Leu657=
ENST00000267163.4:c.1969C>T ENSP00000267163.4:p.Leu657=
NM_000321.2:c.1969C>T , LRG_517t1:c.1969C>T NP_000312.2:p.Leu657=
XM_011535171.1:c.1708C>T XP_011533473.1:p.Leu570=
XM_011535171.2:c.1708C>T XP_011533473.1:p.Leu570=
NM_000321.3:c.1969C>T MANE Select NP_000312.2:p.Leu657=