Canonical Allele Identifier: CA2619265591

Gene: ERBB3

Linked Data

• gnomAD v4: 12-56096868-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.56096868T>C , CM000674.2:g.56096868T>C	GRCh38
NC_000012.11:g.56490652T>C , CM000674.1:g.56490652T>C	GRCh37
NC_000012.10:g.54776919T>C	NCBI36
NG_011529.1:g.21761T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000682431.1:n.3760+22T>C
ENST00000683018.1:c.2097+22T>C	ENSP00000506822.1:n.2097+22T>C
ENST00000683059.1:c.2097+22T>C	ENSP00000507402.1:n.2097+22T>C
ENST00000683164.1:c.2097+22T>C	ENSP00000508051.1:n.2097+22T>C
ENST00000683653.1:n.3007+22T>C
ENST00000684500.1:n.3315+22T>C
ENST00000684766.1:n.517+22T>C
ENST00000267101.8:c.2274+22T>C MANE Select	ENSP00000267101.4:n.2274+22T>C
ENST00000267101.7:c.2274+22T>C	ENSP00000267101.3:n.2274+22T>C
ENST00000415288.6:c.2097+22T>C	ENSP00000408340.2:n.2097+22T>C
ENST00000550070.6:c.537+336T>C	ENSP00000448946.2:n.537+336T>C
ENST00000551085.5:c.2274+22T>C	ENSP00000448483.1:n.2274+22T>C
ENST00000551242.5:c.989-3314T>C	ENSP00000447510.1:n.989-3314T>C
ENST00000553131.5:c.-4+22T>C	ENSP00000449129.1:n.-4+22T>C
NM_001982.3:c.2274+22T>C	NP_001973.2:n.2274+22T>C
NM_001982.4:c.2274+22T>C MANE Select	NP_001973.2:n.2274+22T>C