Canonical Allele Identifier: CA499669424

Gene: ERBB2

Linked Data

• dbSNP Id: rs1481084656
• MyVariant Identifiers: chr17:g.37868197G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39711944G>C , CM000679.2:g.39711944G>C	GRCh38
NC_000017.10:g.37868197G>C , CM000679.1:g.37868197G>C	GRCh37
NC_000017.9:g.35121723G>C	NCBI36
NG_007503.1:g.28805G>C , LRG_724:g.28805G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.918G>C MANE Select	ENSP00000269571.4:p.Thr306=
ENST00000269571.9:c.918G>C	ENSP00000269571.4:p.Thr306=
ENST00000406381.6:c.828G>C	ENSP00000385185.2:p.Thr276=
ENST00000445658.6:c.90G>C	ENSP00000404047.2:p.Thr30=
ENST00000541774.5:c.873G>C	ENSP00000446466.1:p.Thr291=
ENST00000578199.5:c.828G>C	ENSP00000462808.1:p.Thr276=
ENST00000578373.5:c.*708G>C	ENSP00000463427.1:n.*708G>C
ENST00000578502.1:c.143G>C
ENST00000582648.5:c.242G>C	ENSP00000462024.1:p.Arg81Pro
ENST00000582788.5:n.407G>C
ENST00000583038.5:n.1610G>C
ENST00000584450.5:c.918G>C	ENSP00000463714.1:p.Thr306=
ENST00000584601.5:c.828G>C	ENSP00000462438.1:p.Thr276=
ENST00000584908.5:n.930G>C
NM_001005862.2:c.828G>C , LRG_724t1:c.828G>C	NP_001005862.1:p.Thr276=
NM_001289936.1:c.873G>C , LRG_724t4:c.873G>C	NP_001276865.1:p.Thr291=
NM_001289937.1:c.918G>C	NP_001276866.1:p.Thr306=
NM_001289938.1:c.828G>C , LRG_724t3:c.828G>C	NP_001276867.1:p.Thr276=
NM_004448.3:c.918G>C , LRG_724t2:c.918G>C	NP_004439.2:p.Thr306=
NR_110535.1:n.1242G>C
XM_024450641.1:c.1056G>C	XP_024306409.1:p.Thr352=
XM_024450642.1:c.1011G>C	XP_024306410.1:p.Thr337=
XM_024450643.1:c.966G>C	XP_024306411.1:p.Thr322=
NM_001005862.3:c.828G>C	NP_001005862.1:p.Thr276=
NM_001289936.2:c.873G>C	NP_001276865.1:p.Thr291=
NM_001289937.2:c.918G>C	NP_001276866.1:p.Thr306=
NM_001289938.2:c.828G>C	NP_001276867.1:p.Thr276=
NM_001382782.1:c.828G>C	NP_001369711.1:p.Thr276=
NM_001382783.1:c.828G>C	NP_001369712.1:p.Thr276=
NM_001382784.1:c.918G>C	NP_001369713.1:p.Thr306=
NM_001382785.1:c.918G>C	NP_001369714.1:p.Thr306=
NM_001382786.1:c.918G>C	NP_001369715.1:p.Thr306=
NM_001382787.1:c.993G>C	NP_001369716.1:p.Thr331=
NM_001382788.1:c.918G>C	NP_001369717.1:p.Thr306=
NM_001382789.1:c.918G>C	NP_001369718.1:p.Thr306=
NM_001382790.1:c.918G>C	NP_001369719.1:p.Thr306=
NM_001382791.1:c.909G>C	NP_001369720.1:p.Thr303=
NM_001382792.1:c.918G>C	NP_001369721.1:p.Thr306=
NM_001382793.1:c.918G>C	NP_001369722.1:p.Thr306=
NM_001382794.1:c.918G>C	NP_001369723.1:p.Thr306=
NM_001382795.1:c.918G>C	NP_001369724.1:p.Thr306=
NM_001382796.1:c.918G>C	NP_001369725.1:p.Thr306=
NM_001382797.1:c.918G>C	NP_001369726.1:p.Thr306=
NM_001382798.1:c.918G>C	NP_001369727.1:p.Thr306=
NM_001382799.1:c.738G>C	NP_001369728.1:p.Thr246=
NM_001382800.1:c.918G>C	NP_001369729.1:p.Thr306=
NM_001382801.1:c.918G>C	NP_001369730.1:p.Thr306=
NM_001382802.1:c.660G>C	NP_001369731.1:p.Thr220=
NM_001382803.1:c.918G>C	NP_001369732.1:p.Thr306=
NM_001382804.1:c.90G>C	NP_001369733.1:p.Thr30=
NM_001382805.1:c.918G>C	NP_001369734.1:p.Thr306=
NM_001382806.1:c.918G>C	NP_001369735.1:p.Thr306=
NM_004448.4:c.918G>C MANE Select	NP_004439.2:p.Thr306=
NR_110535.2:n.1156G>C