Canonical Allele Identifier: CA2635543257

Gene: ARRB2

Linked Data

• gnomAD v4: 17-4710636-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4710636T>C , CM000679.2:g.4710636T>C	GRCh38
NC_000017.10:g.4613931T>C , CM000679.1:g.4613931T>C	GRCh37
NC_000017.9:g.4560680T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269260.7:c.-86T>C MANE Select	ENSP00000269260.2:n.-86T>C
ENST00000269260.6:c.-86T>C	ENSP00000269260.2:n.-86T>C
ENST00000346341.6:c.-86T>C	ENSP00000341895.2:n.-86T>C
ENST00000570718.5:n.5T>C
ENST00000570739.5:n.5T>C
ENST00000574502.5:c.-86T>C	ENSP00000458371.1:n.-86T>C
ENST00000574954.5:c.-631T>C	ENSP00000466344.1:n.-631T>C
NM_001257328.1:c.-86T>C	NP_001244257.1:n.-86T>C
NM_001257329.1:c.-86T>C	NP_001244258.1:n.-86T>C
NM_001257330.1:c.-86T>C	NP_001244259.1:n.-86T>C
NM_001257331.1:c.-86T>C	NP_001244260.1:n.-86T>C
NM_004313.3:c.-86T>C	NP_004304.1:n.-86T>C
NM_199004.1:c.-86T>C	NP_945355.1:n.-86T>C
NR_047516.1:n.143T>C
XM_006721520.1:c.-586T>C	XP_006721583.1:n.-586T>C
NM_001330064.1:c.-586T>C	NP_001316993.1:n.-586T>C
XM_024450751.1:c.-86T>C	XP_024306519.1:n.-86T>C
XM_024450752.1:c.-631T>C	XP_024306520.1:n.-631T>C
XM_024450753.1:c.-586T>C	XP_024306521.1:n.-586T>C
XR_002958006.1:n.7T>C
XR_002958007.1:n.7T>C
NM_004313.4:c.-86T>C MANE Select	NP_004304.1:n.-86T>C
NM_001257328.2:c.-86T>C	NP_001244257.1:n.-86T>C
NM_001257329.2:c.-86T>C	NP_001244258.1:n.-86T>C
NM_001257330.2:c.-86T>C	NP_001244259.1:n.-86T>C
NM_001257331.2:c.-86T>C	NP_001244260.1:n.-86T>C
NM_001330064.2:c.-586T>C	NP_001316993.1:n.-586T>C
NM_199004.2:c.-86T>C	NP_945355.1:n.-86T>C
NR_047516.2:n.5T>C