Canonical Allele Identifier: CA399310936

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059838531
• MyVariant Identifiers: chr17:g.37883698C>G (hg19) ; chr17:g.39727445C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727445C>G , CM000679.2:g.39727445C>G	GRCh38
NC_000017.10:g.37883698C>G , CM000679.1:g.37883698C>G	GRCh37
NC_000017.9:g.35137224C>G	NCBI36
NG_007503.1:g.44306C>G , LRG_724:g.44306C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3310C>G MANE Select	ENSP00000269571.4:p.His1104Asp
ENST00000269571.9:c.3310C>G	ENSP00000269571.4:p.His1104Asp
ENST00000406381.6:c.3220C>G	ENSP00000385185.2:p.His1074Asp
ENST00000445658.6:c.2482C>G	ENSP00000404047.2:p.His828Asp
ENST00000541774.5:c.3265C>G	ENSP00000446466.1:p.His1089Asp
ENST00000578373.5:c.*3100C>G	ENSP00000463427.1:n.*3100C>G
ENST00000584450.5:c.3160-244C>G	ENSP00000463714.1:n.3160-244C>G
ENST00000584601.5:c.3220C>G	ENSP00000462438.1:p.His1074Asp
NM_001005862.2:c.3220C>G , LRG_724t1:c.3220C>G	NP_001005862.1:p.His1074Asp
NM_001289936.1:c.3265C>G , LRG_724t4:c.3265C>G	NP_001276865.1:p.His1089Asp
NM_001289937.1:c.3160-244C>G	NP_001276866.1:n.3160-244C>G
NM_004448.3:c.3310C>G , LRG_724t2:c.3310C>G	NP_004439.2:p.His1104Asp
NR_110535.1:n.3634C>G
XM_024450641.1:c.3448C>G	XP_024306409.1:p.His1150Asp
XM_024450642.1:c.3403C>G	XP_024306410.1:p.His1135Asp
XM_024450643.1:c.3358C>G	XP_024306411.1:p.His1120Asp
NM_001005862.3:c.3220C>G	NP_001005862.1:p.His1074Asp
NM_001289936.2:c.3265C>G	NP_001276865.1:p.His1089Asp
NM_001289937.2:c.3160-244C>G	NP_001276866.1:n.3160-244C>G
NM_001382782.1:c.3220C>G	NP_001369711.1:p.His1074Asp
NM_001382783.1:c.3220C>G	NP_001369712.1:p.His1074Asp
NM_001382784.1:c.3427C>G	NP_001369713.1:p.His1143Asp
NM_001382785.1:c.3412C>G	NP_001369714.1:p.His1138Asp
NM_001382786.1:c.3391C>G	NP_001369715.1:p.His1131Asp
NM_001382787.1:c.3385C>G	NP_001369716.1:p.His1129Asp
NM_001382788.1:c.3340C>G	NP_001369717.1:p.His1114Asp
NM_001382789.1:c.3331C>G	NP_001369718.1:p.His1111Asp
NM_001382790.1:c.3307C>G	NP_001369719.1:p.His1103Asp
NM_001382791.1:c.3301C>G	NP_001369720.1:p.His1101Asp
NM_001382792.1:c.3274C>G	NP_001369721.1:p.His1092Asp
NM_001382793.1:c.3268C>G	NP_001369722.1:p.His1090Asp
NM_001382794.1:c.3268C>G	NP_001369723.1:p.His1090Asp
NM_001382795.1:c.3262C>G	NP_001369724.1:p.His1088Asp
NM_001382796.1:c.3223C>G	NP_001369725.1:p.His1075Asp
NM_001382797.1:c.3211C>G	NP_001369726.1:p.His1071Asp
NM_001382798.1:c.3154C>G	NP_001369727.1:p.His1052Asp
NM_001382799.1:c.3130C>G	NP_001369728.1:p.His1044Asp
NM_001382800.1:c.3124C>G	NP_001369729.1:p.His1042Asp
NM_001382801.1:c.3106C>G	NP_001369730.1:p.His1036Asp
NM_001382802.1:c.3052C>G	NP_001369731.1:p.His1018Asp
NM_001382803.1:c.3118-244C>G	NP_001369732.1:n.3118-244C>G
NM_001382804.1:c.2482C>G	NP_001369733.1:p.His828Asp
NM_001382805.1:c.2359C>G	NP_001369734.1:p.His787Asp
NM_001382806.1:c.2272C>G	NP_001369735.1:p.His758Asp
NM_004448.4:c.3310C>G MANE Select	NP_004439.2:p.His1104Asp
NR_110535.2:n.3548C>G