Canonical Allele Identifier: CA16602845
Gene: ERBB3 HGNC NCBI

Linked Data

ClinVar Variation Id: 376408
dbSNP Id: rs1057519892

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.56088558A>T , CM000674.2:g.56088558A>T GRCh38
NC_000012.11:g.56482342A>T , CM000674.1:g.56482342A>T GRCh37
NC_000012.10:g.54768609A>T NCBI36
NG_011529.1:g.13451A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000682431.1:n.1049A>T
ENST00000683018.1:c.713A>T ENSP00000506822.1:p.Asp238Val
ENST00000683059.1:c.713A>T ENSP00000507402.1:p.Asp238Val
ENST00000683164.1:c.713A>T ENSP00000508051.1:p.Asp238Val
ENST00000683653.1:n.844A>T
ENST00000684500.1:n.1019A>T
ENST00000267101.8:c.890A>T MANE Select ENSP00000267101.4:p.Asp297Val
ENST00000267101.7:c.890A>T ENSP00000267101.3:p.Asp297Val
ENST00000415288.6:c.713A>T ENSP00000408340.2:p.Asp238Val
ENST00000546748.1:n.355A>T
ENST00000550869.5:c.25-5923A>T ENSP00000448671.1:n.25-5923A>T
ENST00000551085.5:c.890A>T ENSP00000448483.1:p.Asp297Val
ENST00000551242.5:c.890A>T ENSP00000447510.1:p.Asp297Val
NM_001982.3:c.890A>T NP_001973.2:p.Asp297Val
NM_001982.4:c.890A>T MANE Select NP_001973.2:p.Asp297Val