Canonical Allele Identifier: CA287163064
Gene: ARRB2 HGNC NCBI

Linked Data

dbSNP Id: rs952397955
gnomAD v4: 17-4710546-G-A
MyVariant Identifiers: chr17:g.4613841G>A (hg19) chr17:g.4710546G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4710546G>A , CM000679.2:g.4710546G>A GRCh38
NC_000017.10:g.4613841G>A , CM000679.1:g.4613841G>A GRCh37
NC_000017.9:g.4560590G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269260.6:c.-176G>A ENSP00000269260.2:n.-176G>A
NM_001257328.1:c.-176G>A NP_001244257.1:n.-176G>A
NM_001257329.1:c.-176G>A NP_001244258.1:n.-176G>A
NM_001257330.1:c.-176G>A NP_001244259.1:n.-176G>A
NM_001257331.1:c.-176G>A NP_001244260.1:n.-176G>A
NM_004313.3:c.-176G>A NP_004304.1:n.-176G>A
NM_199004.1:c.-176G>A NP_945355.1:n.-176G>A
NR_047516.1:n.53G>A
NM_001330064.1:c.-676G>A NP_001316993.1:n.-676G>A
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