Canonical Allele Identifier: CA287163051
Gene: ARRB2 HGNC NCBI

Linked Data

dbSNP Id: rs1033747459
gnomAD v3: 17-4710535-C-T
gnomAD v4: 17-4710535-C-T
MyVariant Identifiers: chr17:g.4613830C>T (hg19) chr17:g.4710535C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.4710535C>T , CM000679.2:g.4710535C>T GRCh38
NC_000017.10:g.4613830C>T , CM000679.1:g.4613830C>T GRCh37
NC_000017.9:g.4560579C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000269260.6:c.-187C>T ENSP00000269260.2:n.-187C>T
NM_001257328.1:c.-187C>T NP_001244257.1:n.-187C>T
NM_001257329.1:c.-187C>T NP_001244258.1:n.-187C>T
NM_001257330.1:c.-187C>T NP_001244259.1:n.-187C>T
NM_001257331.1:c.-187C>T NP_001244260.1:n.-187C>T
NM_004313.3:c.-187C>T NP_004304.1:n.-187C>T
NM_199004.1:c.-187C>T NP_945355.1:n.-187C>T
NR_047516.1:n.42C>T
NM_001330064.1:c.-687C>T NP_001316993.1:n.-687C>T
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