Canonical Allele Identifier: CA2635543251

Gene: ARRB2

Linked Data

• gnomAD v4: 17-4710630-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4710630G>T , CM000679.2:g.4710630G>T	GRCh38
NC_000017.10:g.4613925G>T , CM000679.1:g.4613925G>T	GRCh37
NC_000017.9:g.4560674G>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269260.6:c.-92G>T	ENSP00000269260.2:n.-92G>T
ENST00000574502.5:c.-92G>T	ENSP00000458371.1:n.-92G>T
ENST00000574954.5:c.-637G>T	ENSP00000466344.1:n.-637G>T
NM_001257328.1:c.-92G>T	NP_001244257.1:n.-92G>T
NM_001257329.1:c.-92G>T	NP_001244258.1:n.-92G>T
NM_001257330.1:c.-92G>T	NP_001244259.1:n.-92G>T
NM_001257331.1:c.-92G>T	NP_001244260.1:n.-92G>T
NM_004313.3:c.-92G>T	NP_004304.1:n.-92G>T
NM_199004.1:c.-92G>T	NP_945355.1:n.-92G>T
NR_047516.1:n.137G>T
NM_001330064.1:c.-592G>T	NP_001316993.1:n.-592G>T
XM_024450751.1:c.-92G>T	XP_024306519.1:n.-92G>T
XM_024450752.1:c.-637G>T	XP_024306520.1:n.-637G>T
XR_002958006.1:n.1G>T
XR_002958007.1:n.1G>T