Canonical Allele Identifier: CA287163113

Gene: ARRB2

Linked Data

• dbSNP Id: rs948802675
• gnomAD v4: 17-4710631-C-T
• MyVariant Identifiers: chr17:g.4613926C>T (hg19) ; chr17:g.4710631C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.4710631C>T , CM000679.2:g.4710631C>T	GRCh38
NC_000017.10:g.4613926C>T , CM000679.1:g.4613926C>T	GRCh37
NC_000017.9:g.4560675C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269260.6:c.-91C>T	ENSP00000269260.2:n.-91C>T
ENST00000574502.5:c.-91C>T	ENSP00000458371.1:n.-91C>T
ENST00000574954.5:c.-636C>T	ENSP00000466344.1:n.-636C>T
NM_001257328.1:c.-91C>T	NP_001244257.1:n.-91C>T
NM_001257329.1:c.-91C>T	NP_001244258.1:n.-91C>T
NM_001257330.1:c.-91C>T	NP_001244259.1:n.-91C>T
NM_001257331.1:c.-91C>T	NP_001244260.1:n.-91C>T
NM_004313.3:c.-91C>T	NP_004304.1:n.-91C>T
NM_199004.1:c.-91C>T	NP_945355.1:n.-91C>T
NR_047516.1:n.138C>T
NM_001330064.1:c.-591C>T	NP_001316993.1:n.-591C>T
XM_024450751.1:c.-91C>T	XP_024306519.1:n.-91C>T
XM_024450752.1:c.-636C>T	XP_024306520.1:n.-636C>T
XR_002958006.1:n.2C>T
XR_002958007.1:n.2C>T