Canonical Allele Identifier: CA388163624

Gene: RB1

Linked Data

• MyVariant Identifiers: chr13:g.48955467T>C (hg19) ; chr13:g.48381331T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48381331T>C , CM000675.2:g.48381331T>C	GRCh38
NC_000013.10:g.48955467T>C , CM000675.1:g.48955467T>C	GRCh37
NC_000013.9:g.47853468T>C	NCBI36
NG_009009.1:g.82585T>C , LRG_517:g.82585T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.1583T>C MANE Select	ENSP00000267163.4:p.Phe528Ser
ENST00000643064.1:c.82T>C
ENST00000650461.1:c.1583T>C	ENSP00000497193.1:p.Phe528Ser
ENST00000267163.4:c.1583T>C	ENSP00000267163.4:p.Phe528Ser
NM_000321.2:c.1583T>C , LRG_517t1:c.1583T>C	NP_000312.2:p.Phe528Ser
XM_011535171.1:c.1322T>C	XP_011533473.1:p.Phe441Ser
XM_011535171.2:c.1322T>C	XP_011533473.1:p.Phe441Ser
NM_000321.3:c.1583T>C MANE Select	NP_000312.2:p.Phe528Ser