Canonical Allele Identifier: CA2619264501

Gene: ERBB3

Linked Data

• gnomAD v4: 12-56088209-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56088209A>C , CM000674.2:g.56088209A>C	GRCh38
NC_000012.11:g.56481993A>C , CM000674.1:g.56481993A>C	GRCh37
NC_000012.10:g.54768260A>C	NCBI36
NG_011529.1:g.13102A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682431.1:n.1033+47A>C
ENST00000683018.1:c.697+47A>C	ENSP00000506822.1:n.697+47A>C
ENST00000683059.1:c.697+47A>C	ENSP00000507402.1:n.697+47A>C
ENST00000683164.1:c.697+47A>C	ENSP00000508051.1:n.697+47A>C
ENST00000683653.1:n.828+47A>C
ENST00000684500.1:n.1003+47A>C
ENST00000267101.8:c.874+47A>C MANE Select	ENSP00000267101.4:n.874+47A>C
ENST00000267101.7:c.874+47A>C	ENSP00000267101.3:n.874+47A>C
ENST00000415288.6:c.697+47A>C	ENSP00000408340.2:n.697+47A>C
ENST00000546748.1:n.339+47A>C
ENST00000550869.5:c.25-6272A>C	ENSP00000448671.1:n.25-6272A>C
ENST00000551085.5:c.874+47A>C	ENSP00000448483.1:n.874+47A>C
ENST00000551242.5:c.874+47A>C	ENSP00000447510.1:n.874+47A>C
NM_001982.3:c.874+47A>C	NP_001973.2:n.874+47A>C
NM_001982.4:c.874+47A>C MANE Select	NP_001973.2:n.874+47A>C