Canonical Allele Identifier: CA2622985050
Gene: RB1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.48459581A>T , CM000675.2:g.48459581A>T GRCh38
NC_000013.10:g.49033717A>T , CM000675.1:g.49033717A>T GRCh37
NC_000013.9:g.47931718A>T NCBI36
NG_009009.1:g.160835A>T , LRG_517:g.160835A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000267163.6:c.1961-107A>T MANE Select ENSP00000267163.4:n.1961-107A>T
ENST00000643064.1:c.194+78138A>T
ENST00000650461.1:c.1961-107A>T ENSP00000497193.1:n.1961-107A>T
ENST00000267163.4:c.1961-107A>T ENSP00000267163.4:n.1961-107A>T
NM_000321.2:c.1961-107A>T , LRG_517t1:c.1961-107A>T NP_000312.2:n.1961-107A>T
XM_011535171.1:c.1700-107A>T XP_011533473.1:n.1700-107A>T
XM_011535171.2:c.1700-107A>T XP_011533473.1:n.1700-107A>T
NM_000321.3:c.1961-107A>T MANE Select NP_000312.2:n.1961-107A>T