Canonical Allele Identifier: CA2726284629

Gene: ERBB3

Linked Data

• dbSNP Id: rs2136817839

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56096865G>A , CM000674.2:g.56096865G>A	GRCh38
NC_000012.11:g.56490649G>A , CM000674.1:g.56490649G>A	GRCh37
NC_000012.10:g.54776916G>A	NCBI36
NG_011529.1:g.21758G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000682431.1:n.3760+19G>A
ENST00000683018.1:c.2097+19G>A	ENSP00000506822.1:n.2097+19G>A
ENST00000683059.1:c.2097+19G>A	ENSP00000507402.1:n.2097+19G>A
ENST00000683164.1:c.2097+19G>A	ENSP00000508051.1:n.2097+19G>A
ENST00000683653.1:n.3007+19G>A
ENST00000684500.1:n.3315+19G>A
ENST00000684766.1:n.517+19G>A
ENST00000267101.8:c.2274+19G>A MANE Select	ENSP00000267101.4:n.2274+19G>A
ENST00000267101.7:c.2274+19G>A	ENSP00000267101.3:n.2274+19G>A
ENST00000415288.6:c.2097+19G>A	ENSP00000408340.2:n.2097+19G>A
ENST00000550070.6:c.537+333G>A	ENSP00000448946.2:n.537+333G>A
ENST00000551085.5:c.2274+19G>A	ENSP00000448483.1:n.2274+19G>A
ENST00000551242.5:c.989-3317G>A	ENSP00000447510.1:n.989-3317G>A
ENST00000553131.5:c.-4+19G>A	ENSP00000449129.1:n.-4+19G>A
NM_001982.3:c.2274+19G>A	NP_001973.2:n.2274+19G>A
NM_001982.4:c.2274+19G>A MANE Select	NP_001973.2:n.2274+19G>A