Canonical Allele Identifier: CA2089982347
Gene: RB1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48364879C= , CM000675.2:g.48364879C= GRCh38
NC_000013.10:g.48939015C= , CM000675.1:g.48939015C= GRCh37
NC_000013.9:g.47837016C= NCBI36
NG_009009.1:g.66133C= , LRG_517:g.66133C=

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.862-15C= MANE Select ENSP00000267163.4:n.862-15C=
ENST00000650461.1:c.862-15C= ENSP00000497193.1:n.862-15C=
ENST00000267163.4:c.862-15C= ENSP00000267163.4:n.862-15C=
NM_000321.2:c.862-15C= , LRG_517t1:c.862-15C= NP_000312.2:n.862-15C=
XM_011535171.1:c.601-15C= XP_011533473.1:n.601-15C=
XM_011535171.2:c.601-15C= XP_011533473.1:n.601-15C=
NM_000321.3:c.862-15C= MANE Select NP_000312.2:n.862-15C=
Search 100 bp 5'
Search 100 bp 3'