Canonical Allele Identifier: CA772513624
Gene: ARRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1457134369
gnomAD v3: 17-4710550-A-G
gnomAD v4: 17-4710550-A-G
MyVariant Identifiers: chr17:g.4613845A>G (hg19) chr17:g.4710550A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4710550A>G , CM000679.2:g.4710550A>G GRCh38
NC_000017.10:g.4613845A>G , CM000679.1:g.4613845A>G GRCh37
NC_000017.9:g.4560594A>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269260.6:c.-172A>G ENSP00000269260.2:n.-172A>G
NM_001257328.1:c.-172A>G NP_001244257.1:n.-172A>G
NM_001257329.1:c.-172A>G NP_001244258.1:n.-172A>G
NM_001257330.1:c.-172A>G NP_001244259.1:n.-172A>G
NM_001257331.1:c.-172A>G NP_001244260.1:n.-172A>G
NM_004313.3:c.-172A>G NP_004304.1:n.-172A>G
NM_199004.1:c.-172A>G NP_945355.1:n.-172A>G
NR_047516.1:n.57A>G
NM_001330064.1:c.-672A>G NP_001316993.1:n.-672A>G
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