Canonical Allele Identifier: CA399314049

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059868968
• gnomAD v4: 17-39727898-C-T
• MyVariant Identifiers: chr17:g.37884151C>T (hg19) ; chr17:g.39727898C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727898C>T , CM000679.2:g.39727898C>T	GRCh38
NC_000017.10:g.37884151C>T , CM000679.1:g.37884151C>T	GRCh37
NC_000017.9:g.35137677C>T	NCBI36
NG_007503.1:g.44759C>T , LRG_724:g.44759C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3622C>T MANE Select	ENSP00000269571.4:p.His1208Tyr
ENST00000269571.9:c.3622C>T	ENSP00000269571.4:p.His1208Tyr
ENST00000406381.6:c.3532C>T	ENSP00000385185.2:p.His1178Tyr
ENST00000445658.6:c.2794C>T	ENSP00000404047.2:p.His932Tyr
ENST00000541774.5:c.3577C>T	ENSP00000446466.1:p.His1193Tyr
ENST00000578373.5:c.*3412C>T	ENSP00000463427.1:n.*3412C>T
ENST00000584450.5:c.*201C>T	ENSP00000463714.1:n.*201C>T
ENST00000584601.5:c.3532C>T	ENSP00000462438.1:p.His1178Tyr
NM_001005862.2:c.3532C>T , LRG_724t1:c.3532C>T	NP_001005862.1:p.His1178Tyr
NM_001289936.1:c.3577C>T , LRG_724t4:c.3577C>T	NP_001276865.1:p.His1193Tyr
NM_001289937.1:c.*201C>T	NP_001276866.1:n.*201C>T
NM_004448.3:c.3622C>T , LRG_724t2:c.3622C>T	NP_004439.2:p.His1208Tyr
NR_110535.1:n.3946C>T
XM_024450641.1:c.3760C>T	XP_024306409.1:p.His1254Tyr
XM_024450642.1:c.3715C>T	XP_024306410.1:p.His1239Tyr
XM_024450643.1:c.3670C>T	XP_024306411.1:p.His1224Tyr
NM_001005862.3:c.3532C>T	NP_001005862.1:p.His1178Tyr
NM_001289936.2:c.3577C>T	NP_001276865.1:p.His1193Tyr
NM_001289937.2:c.*201C>T	NP_001276866.1:n.*201C>T
NM_001382782.1:c.3532C>T	NP_001369711.1:p.His1178Tyr
NM_001382783.1:c.3532C>T	NP_001369712.1:p.His1178Tyr
NM_001382784.1:c.3739C>T	NP_001369713.1:p.His1247Tyr
NM_001382785.1:c.3724C>T	NP_001369714.1:p.His1242Tyr
NM_001382786.1:c.3703C>T	NP_001369715.1:p.His1235Tyr
NM_001382787.1:c.3697C>T	NP_001369716.1:p.His1233Tyr
NM_001382788.1:c.3652C>T	NP_001369717.1:p.His1218Tyr
NM_001382789.1:c.3643C>T	NP_001369718.1:p.His1215Tyr
NM_001382790.1:c.3619C>T	NP_001369719.1:p.His1207Tyr
NM_001382791.1:c.3613C>T	NP_001369720.1:p.His1205Tyr
NM_001382792.1:c.3586C>T	NP_001369721.1:p.His1196Tyr
NM_001382793.1:c.3580C>T	NP_001369722.1:p.His1194Tyr
NM_001382794.1:c.3580C>T	NP_001369723.1:p.His1194Tyr
NM_001382795.1:c.3574C>T	NP_001369724.1:p.His1192Tyr
NM_001382796.1:c.3535C>T	NP_001369725.1:p.His1179Tyr
NM_001382797.1:c.3523C>T	NP_001369726.1:p.His1175Tyr
NM_001382798.1:c.3466C>T	NP_001369727.1:p.His1156Tyr
NM_001382799.1:c.3442C>T	NP_001369728.1:p.His1148Tyr
NM_001382800.1:c.3436C>T	NP_001369729.1:p.His1146Tyr
NM_001382801.1:c.3418C>T	NP_001369730.1:p.His1140Tyr
NM_001382802.1:c.3364C>T	NP_001369731.1:p.His1122Tyr
NM_001382803.1:c.*201C>T	NP_001369732.1:n.*201C>T
NM_001382804.1:c.2794C>T	NP_001369733.1:p.His932Tyr
NM_001382805.1:c.2671C>T	NP_001369734.1:p.His891Tyr
NM_001382806.1:c.2584C>T	NP_001369735.1:p.His862Tyr
NM_004448.4:c.3622C>T MANE Select	NP_004439.2:p.His1208Tyr
NR_110535.2:n.3860C>T