Canonical Allele Identifier: CA13464499

Gene: ARRB1

Linked Data

• dbSNP Id: rs472112
• gnomAD v2: 11-75021501-C-T
• gnomAD v3: 11-75310457-C-T
• gnomAD v4: 11-75310457-C-T
• MyVariant Identifiers: chr11:g.75021501C>T (hg19) ; chr11:g.75310457C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.75310457C>T , CM000673.2:g.75310457C>T	GRCh38
NC_000011.9:g.75021501C>T , CM000673.1:g.75021501C>T	GRCh37
NC_000011.8:g.74699149C>T	NCBI36
NG_028118.1:g.46375G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000420843.7:c.21-20418G>A MANE Select	ENSP00000409581.2:n.21-20418G>A
ENST00000360025.7:c.21-20418G>A	ENSP00000353124.3:n.21-20418G>A
ENST00000420843.6:c.21-20418G>A	ENSP00000409581.2:n.21-20418G>A
ENST00000524400.5:c.94+1605G>A
ENST00000533255.1:n.74-20418G>A
ENST00000533609.5:c.63+1605G>A	ENSP00000436352.1:n.63+1605G>A
NM_004041.4:c.21-20418G>A	NP_004032.2:n.21-20418G>A
NM_020251.3:c.21-20418G>A	NP_064647.1:n.21-20418G>A
XM_005273997.1:c.32+1605G>A	XP_005274054.1:n.32+1605G>A
XM_011545034.1:c.33-150G>A	XP_011543336.1:n.33-150G>A
XM_011545035.1:c.33-150G>A	XP_011543337.1:n.33-150G>A
XM_011545034.2:c.33-150G>A	XP_011543336.1:n.33-150G>A
XM_011545035.2:c.33-150G>A	XP_011543337.1:n.33-150G>A
XM_017017750.1:c.33-150G>A	XP_016873239.1:n.33-150G>A
XM_017017751.1:c.33-150G>A	XP_016873240.1:n.33-150G>A
XM_017017752.2:c.21-20418G>A	XP_016873241.1:n.21-20418G>A
XM_017017754.2:c.21-20418G>A	XP_016873243.1:n.21-20418G>A
NM_004041.5:c.21-20418G>A MANE Select	NP_004032.2:n.21-20418G>A
NM_020251.4:c.21-20418G>A	NP_064647.1:n.21-20418G>A