Canonical Allele Identifier: CA6622060

Gene: ERBB3

Linked Data

• ClinVar Variation Id: 1316296
• ClinVar RCV Id: RCV001766202
• dbSNP Id: rs78663322
• ExAC: 12:56481775 A / G
• gnomAD v2: 12-56481775-A-G
• gnomAD v3: 12-56087991-A-G
• gnomAD v4: 12-56087991-A-G
• MyVariant Identifiers: chr12:g.56481775A>G (hg19) ; chr12:g.56087991A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56087991A>G , CM000674.2:g.56087991A>G	GRCh38
NC_000012.11:g.56481775A>G , CM000674.1:g.56481775A>G	GRCh37
NC_000012.10:g.54768042A>G	NCBI36
NG_011529.1:g.12884A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000682431.1:n.892-30A>G
ENST00000683018.1:c.556-30A>G	ENSP00000506822.1:n.556-30A>G
ENST00000683059.1:c.556-30A>G	ENSP00000507402.1:n.556-30A>G
ENST00000683164.1:c.556-30A>G	ENSP00000508051.1:n.556-30A>G
ENST00000683653.1:n.687-30A>G
ENST00000684500.1:n.862-30A>G
ENST00000267101.8:c.733-30A>G MANE Select	ENSP00000267101.4:n.733-30A>G
ENST00000267101.7:c.733-30A>G	ENSP00000267101.3:n.733-30A>G
ENST00000415288.6:c.556-30A>G	ENSP00000408340.2:n.556-30A>G
ENST00000546748.1:n.168A>G
ENST00000549472.1:n.476-30A>G
ENST00000550869.5:c.25-6490A>G	ENSP00000448671.1:n.25-6490A>G
ENST00000551085.5:c.733-30A>G	ENSP00000448483.1:n.733-30A>G
ENST00000551242.5:c.733-30A>G	ENSP00000447510.1:n.733-30A>G
NM_001982.3:c.733-30A>G	NP_001973.2:n.733-30A>G
NM_001982.4:c.733-30A>G MANE Select	NP_001973.2:n.733-30A>G