Canonical Allele Identifier: CA772513645
Gene: ARRB2 HGNC NCBI

Linked Data

dbSNP Id: rs984705308
gnomAD v3: 17-4710572-A-C
gnomAD v4: 17-4710572-A-C
MyVariant Identifiers: chr17:g.4613867A>C (hg19) chr17:g.4710572A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4710572A>C , CM000679.2:g.4710572A>C GRCh38
NC_000017.10:g.4613867A>C , CM000679.1:g.4613867A>C GRCh37
NC_000017.9:g.4560616A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269260.6:c.-150A>C ENSP00000269260.2:n.-150A>C
NM_001257328.1:c.-150A>C NP_001244257.1:n.-150A>C
NM_001257329.1:c.-150A>C NP_001244258.1:n.-150A>C
NM_001257330.1:c.-150A>C NP_001244259.1:n.-150A>C
NM_001257331.1:c.-150A>C NP_001244260.1:n.-150A>C
NM_004313.3:c.-150A>C NP_004304.1:n.-150A>C
NM_199004.1:c.-150A>C NP_945355.1:n.-150A>C
NR_047516.1:n.79A>C
NM_001330064.1:c.-650A>C NP_001316993.1:n.-650A>C
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