Canonical Allele Identifier: CA2244513979
Gene: ARRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1914280393
gnomAD v4: 17-4710596-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4710596A>G , CM000679.2:g.4710596A>G GRCh38
NC_000017.10:g.4613891A>G , CM000679.1:g.4613891A>G GRCh37
NC_000017.9:g.4560640A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269260.6:c.-126A>G ENSP00000269260.2:n.-126A>G
ENST00000574502.5:c.-126A>G ENSP00000458371.1:n.-126A>G
NM_001257328.1:c.-126A>G NP_001244257.1:n.-126A>G
NM_001257329.1:c.-126A>G NP_001244258.1:n.-126A>G
NM_001257330.1:c.-126A>G NP_001244259.1:n.-126A>G
NM_001257331.1:c.-126A>G NP_001244260.1:n.-126A>G
NM_004313.3:c.-126A>G NP_004304.1:n.-126A>G
NM_199004.1:c.-126A>G NP_945355.1:n.-126A>G
NR_047516.1:n.103A>G
NM_001330064.1:c.-626A>G NP_001316993.1:n.-626A>G