Canonical Allele Identifier: CA3751999
Gene: RXRB HGNC NCBI

Linked Data

dbSNP Id: rs2076310
gnomAD v2: 6-33166034-A-G
gnomAD v3: 6-33198257-A-G
gnomAD v4: 6-33198257-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.33198257A>G , CM000668.2:g.33198257A>G GRCh38
NC_000006.11:g.33166034A>G , CM000668.1:g.33166034A>G GRCh37
NC_000006.10:g.33274012A>G NCBI36
NG_023374.1:g.7399T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000374680.4:c.640+51T>C MANE Select ENSP00000363812.3:n.640+51T>C
ENST00000374680.3:c.640+51T>C ENSP00000363812.3:n.640+51T>C
ENST00000374685.8:c.640+51T>C ENSP00000363817.4:n.640+51T>C
ENST00000481441.1:n.328+51T>C
ENST00000483281.5:c.*152+51T>C ENSP00000431369.1:n.*152+51T>C
NM_001270401.1:c.640+51T>C NP_001257330.1:n.640+51T>C
NM_001291989.1:c.70+51T>C NP_001278918.1:n.70+51T>C
NM_021976.4:c.640+51T>C NP_068811.1:n.640+51T>C
XM_005249278.1:c.352+51T>C XP_005249335.1:n.352+51T>C
XM_005249279.1:c.352+51T>C XP_005249336.1:n.352+51T>C
XM_011514796.1:c.289+51T>C XP_011513098.1:n.289+51T>C
XR_926297.1:n.836+51T>C
XM_005249278.3:c.352+51T>C XP_005249335.1:n.352+51T>C
XM_011514796.3:c.289+51T>C XP_011513098.1:n.289+51T>C
XM_017011176.1:c.271+51T>C XP_016866665.1:n.271+51T>C
NM_001270401.2:c.640+51T>C NP_001257330.1:n.640+51T>C
NM_021976.5:c.640+51T>C MANE Select NP_068811.1:n.640+51T>C
NM_001291989.2:c.70+51T>C NP_001278918.1:n.70+51T>C