Canonical Allele Identifier: CA2635543162

Gene: ARRB2

Linked Data

• gnomAD v4: 17-4710567-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4710567T>C , CM000679.2:g.4710567T>C	GRCh38
NC_000017.10:g.4613862T>C , CM000679.1:g.4613862T>C	GRCh37
NC_000017.9:g.4560611T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269260.6:c.-155T>C	ENSP00000269260.2:n.-155T>C
NM_001257328.1:c.-155T>C	NP_001244257.1:n.-155T>C
NM_001257329.1:c.-155T>C	NP_001244258.1:n.-155T>C
NM_001257330.1:c.-155T>C	NP_001244259.1:n.-155T>C
NM_001257331.1:c.-155T>C	NP_001244260.1:n.-155T>C
NM_004313.3:c.-155T>C	NP_004304.1:n.-155T>C
NM_199004.1:c.-155T>C	NP_945355.1:n.-155T>C
NR_047516.1:n.74T>C
NM_001330064.1:c.-655T>C	NP_001316993.1:n.-655T>C