Canonical Allele Identifier: CA6622565

Gene: ERBB3

Linked Data

• dbSNP Id: rs764987438
• ExAC: 12:56490655 C / G
• gnomAD v2: 12-56490655-C-G
• gnomAD v4: 12-56096871-C-G
• MyVariant Identifiers: chr12:g.56490655C>G (hg19) ; chr12:g.56096871C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56096871C>G , CM000674.2:g.56096871C>G	GRCh38
NC_000012.11:g.56490655C>G , CM000674.1:g.56490655C>G	GRCh37
NC_000012.10:g.54776922C>G	NCBI36
NG_011529.1:g.21764C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000682431.1:n.3760+25C>G
ENST00000683018.1:c.2097+25C>G	ENSP00000506822.1:n.2097+25C>G
ENST00000683059.1:c.2097+25C>G	ENSP00000507402.1:n.2097+25C>G
ENST00000683164.1:c.2097+25C>G	ENSP00000508051.1:n.2097+25C>G
ENST00000683653.1:n.3007+25C>G
ENST00000684500.1:n.3315+25C>G
ENST00000684766.1:n.517+25C>G
ENST00000267101.8:c.2274+25C>G MANE Select	ENSP00000267101.4:n.2274+25C>G
ENST00000267101.7:c.2274+25C>G	ENSP00000267101.3:n.2274+25C>G
ENST00000415288.6:c.2097+25C>G	ENSP00000408340.2:n.2097+25C>G
ENST00000550070.6:c.537+339C>G	ENSP00000448946.2:n.537+339C>G
ENST00000551085.5:c.2274+25C>G	ENSP00000448483.1:n.2274+25C>G
ENST00000551242.5:c.989-3311C>G	ENSP00000447510.1:n.989-3311C>G
ENST00000553131.5:c.-4+25C>G	ENSP00000449129.1:n.-4+25C>G
NM_001982.3:c.2274+25C>G	NP_001973.2:n.2274+25C>G
NM_001982.4:c.2274+25C>G MANE Select	NP_001973.2:n.2274+25C>G