Canonical Allele Identifier: CA388166692

Gene: RB1

Linked Data

• dbSNP Id: rs751799266
• MyVariant Identifiers: chr13:g.49033839A>C (hg19) ; chr13:g.48459703A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48459703A>C , CM000675.2:g.48459703A>C	GRCh38
NC_000013.10:g.49033839A>C , CM000675.1:g.49033839A>C	GRCh37
NC_000013.9:g.47931840A>C	NCBI36
NG_009009.1:g.160957A>C , LRG_517:g.160957A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.1976A>C MANE Select	ENSP00000267163.4:p.Tyr659Ser
ENST00000643064.1:c.194+78260A>C
ENST00000650461.1:c.1976A>C	ENSP00000497193.1:p.Tyr659Ser
ENST00000267163.4:c.1976A>C	ENSP00000267163.4:p.Tyr659Ser
NM_000321.2:c.1976A>C , LRG_517t1:c.1976A>C	NP_000312.2:p.Tyr659Ser
XM_011535171.1:c.1715A>C	XP_011533473.1:p.Tyr572Ser
XM_011535171.2:c.1715A>C	XP_011533473.1:p.Tyr572Ser
NM_000321.3:c.1976A>C MANE Select	NP_000312.2:p.Tyr659Ser