Canonical Allele Identifier: CA480366697

Gene: ERBB3

Linked Data

• MyVariant Identifiers: chr12:g.56481834C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56088050C>G , CM000674.2:g.56088050C>G	GRCh38
NC_000012.11:g.56481834C>G , CM000674.1:g.56481834C>G	GRCh37
NC_000012.10:g.54768101C>G	NCBI36
NG_011529.1:g.12943C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682431.1:n.921C>G
ENST00000683018.1:c.585C>G	ENSP00000506822.1:p.Ala195=
ENST00000683059.1:c.585C>G	ENSP00000507402.1:p.Ala195=
ENST00000683164.1:c.585C>G	ENSP00000508051.1:p.Ala195=
ENST00000683653.1:n.716C>G
ENST00000684500.1:n.891C>G
ENST00000267101.8:c.762C>G MANE Select	ENSP00000267101.4:p.Ala254=
ENST00000267101.7:c.762C>G	ENSP00000267101.3:p.Ala254=
ENST00000415288.6:c.585C>G	ENSP00000408340.2:p.Ala195=
ENST00000546748.1:n.227C>G
ENST00000549472.1:n.505C>G
ENST00000550869.5:c.25-6431C>G	ENSP00000448671.1:n.25-6431C>G
ENST00000551085.5:c.762C>G	ENSP00000448483.1:p.Ala254=
ENST00000551242.5:c.762C>G	ENSP00000447510.1:p.Ala254=
NM_001982.3:c.762C>G	NP_001973.2:p.Ala254=
NM_001982.4:c.762C>G MANE Select	NP_001973.2:p.Ala254=