Canonical Allele Identifier: CA1983269493

Gene: ARRB1

Genomic Alleles

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

Transcript Alleles

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