Canonical Allele Identifier: CA2575413701
Gene: RB1 HGNC NCBI

Linked Data

dbSNP Id: rs2138359964

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48476910A>G , CM000675.2:g.48476910A>G GRCh38
NC_000013.10:g.49051046A>G , CM000675.1:g.49051046A>G GRCh37
NC_000013.9:g.47949047A>G NCBI36
NG_009009.1:g.178164A>G , LRG_517:g.178164A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000267163.6:c.2663+67A>G MANE Select ENSP00000267163.4:n.2663+67A>G
ENST00000643064.1:c.194+95467A>G
ENST00000650461.1:c.2663+67A>G ENSP00000497193.1:n.2663+67A>G
ENST00000267163.4:c.2663+67A>G ENSP00000267163.4:n.2663+67A>G
ENST00000484879.1:n.397+67A>G
ENST00000531171.5:n.266+67A>G
NM_000321.2:c.2663+67A>G , LRG_517t1:c.2663+67A>G NP_000312.2:n.2663+67A>G
XM_011535171.1:c.2402+67A>G XP_011533473.1:n.2402+67A>G
XM_011535171.2:c.2402+67A>G XP_011533473.1:n.2402+67A>G
NM_000321.3:c.2663+67A>G MANE Select NP_000312.2:n.2663+67A>G