Canonical Allele Identifier: CA2619264570

Gene: ERBB3

Linked Data

• gnomAD v4: 12-56088394-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56088394T>A , CM000674.2:g.56088394T>A	GRCh38
NC_000012.11:g.56482178T>A , CM000674.1:g.56482178T>A	GRCh37
NC_000012.10:g.54768445T>A	NCBI36
NG_011529.1:g.13287T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682431.1:n.1034-149T>A
ENST00000683018.1:c.698-149T>A	ENSP00000506822.1:n.698-149T>A
ENST00000683059.1:c.698-149T>A	ENSP00000507402.1:n.698-149T>A
ENST00000683164.1:c.698-149T>A	ENSP00000508051.1:n.698-149T>A
ENST00000683653.1:n.829-149T>A
ENST00000684500.1:n.1004-149T>A
ENST00000267101.8:c.875-149T>A MANE Select	ENSP00000267101.4:n.875-149T>A
ENST00000267101.7:c.875-149T>A	ENSP00000267101.3:n.875-149T>A
ENST00000415288.6:c.698-149T>A	ENSP00000408340.2:n.698-149T>A
ENST00000546748.1:n.340-149T>A
ENST00000550869.5:c.25-6087T>A	ENSP00000448671.1:n.25-6087T>A
ENST00000551085.5:c.875-149T>A	ENSP00000448483.1:n.875-149T>A
ENST00000551242.5:c.875-149T>A	ENSP00000447510.1:n.875-149T>A
NM_001982.3:c.875-149T>A	NP_001973.2:n.875-149T>A
NM_001982.4:c.875-149T>A MANE Select	NP_001973.2:n.875-149T>A