Canonical Allele Identifier: CA249269220

Gene: RB1

Linked Data

• dbSNP Id: rs1029631740
• gnomAD v3: 13-48348647-T-C
• gnomAD v4: 13-48348647-T-C
• MyVariant Identifiers: chr13:g.48922783T>C (hg19) ; chr13:g.48348647T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.48348647T>C , CM000675.2:g.48348647T>C	GRCh38
NC_000013.10:g.48922783T>C , CM000675.1:g.48922783T>C	GRCh37
NC_000013.9:g.47820784T>C	NCBI36
NG_009009.1:g.49901T>C , LRG_517:g.49901T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000267163.6:c.540-309T>C MANE Select	ENSP00000267163.4:n.540-309T>C
ENST00000650461.1:c.540-309T>C	ENSP00000497193.1:n.540-309T>C
ENST00000267163.4:c.540-309T>C	ENSP00000267163.4:n.540-309T>C
ENST00000467505.5:c.138-11370T>C	ENSP00000434702.1:n.138-11370T>C
ENST00000525036.1:n.702-309T>C
NM_000321.2:c.540-309T>C , LRG_517t1:c.540-309T>C	NP_000312.2:n.540-309T>C
XM_011535171.1:c.279-309T>C	XP_011533473.1:n.279-309T>C
XM_011535171.2:c.279-309T>C	XP_011533473.1:n.279-309T>C
NM_000321.3:c.540-309T>C MANE Select	NP_000312.2:n.540-309T>C