Canonical Allele Identifier: CA2619264373

Gene: ERBB3

Linked Data

• gnomAD v4: 12-56088013-T-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56088013T>A , CM000674.2:g.56088013T>A	GRCh38
NC_000012.11:g.56481797T>A , CM000674.1:g.56481797T>A	GRCh37
NC_000012.10:g.54768064T>A	NCBI36
NG_011529.1:g.12906T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682431.1:n.892-8T>A
ENST00000683018.1:c.556-8T>A	ENSP00000506822.1:n.556-8T>A
ENST00000683059.1:c.556-8T>A	ENSP00000507402.1:n.556-8T>A
ENST00000683164.1:c.556-8T>A	ENSP00000508051.1:n.556-8T>A
ENST00000683653.1:n.687-8T>A
ENST00000684500.1:n.862-8T>A
ENST00000267101.8:c.733-8T>A MANE Select	ENSP00000267101.4:n.733-8T>A
ENST00000267101.7:c.733-8T>A	ENSP00000267101.3:n.733-8T>A
ENST00000415288.6:c.556-8T>A	ENSP00000408340.2:n.556-8T>A
ENST00000546748.1:n.190T>A
ENST00000549472.1:n.476-8T>A
ENST00000550869.5:c.25-6468T>A	ENSP00000448671.1:n.25-6468T>A
ENST00000551085.5:c.733-8T>A	ENSP00000448483.1:n.733-8T>A
ENST00000551242.5:c.733-8T>A	ENSP00000447510.1:n.733-8T>A
NM_001982.3:c.733-8T>A	NP_001973.2:n.733-8T>A
NM_001982.4:c.733-8T>A MANE Select	NP_001973.2:n.733-8T>A