Canonical Allele Identifier: CA287163056
Gene: ARRB2 HGNC NCBI

Linked Data

dbSNP Id: rs576221896
gnomAD v2: 17-4613832-C-G
gnomAD v3: 17-4710537-C-G
gnomAD v4: 17-4710537-C-G
MyVariant Identifiers: chr17:g.4613832C>G (hg19) chr17:g.4710537C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4710537C>G , CM000679.2:g.4710537C>G GRCh38
NC_000017.10:g.4613832C>G , CM000679.1:g.4613832C>G GRCh37
NC_000017.9:g.4560581C>G NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269260.6:c.-185C>G ENSP00000269260.2:n.-185C>G
NM_001257328.1:c.-185C>G NP_001244257.1:n.-185C>G
NM_001257329.1:c.-185C>G NP_001244258.1:n.-185C>G
NM_001257330.1:c.-185C>G NP_001244259.1:n.-185C>G
NM_001257331.1:c.-185C>G NP_001244260.1:n.-185C>G
NM_004313.3:c.-185C>G NP_004304.1:n.-185C>G
NM_199004.1:c.-185C>G NP_945355.1:n.-185C>G
NR_047516.1:n.44C>G
NM_001330064.1:c.-685C>G NP_001316993.1:n.-685C>G
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