Canonical Allele Identifier: CA399310956

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143249422
• MyVariant Identifiers: chr17:g.37883700T>G (hg19) ; chr17:g.39727447T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727447T>G , CM000679.2:g.39727447T>G	GRCh38
NC_000017.10:g.37883700T>G , CM000679.1:g.37883700T>G	GRCh37
NC_000017.9:g.35137226T>G	NCBI36
NG_007503.1:g.44308T>G , LRG_724:g.44308T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3312T>G MANE Select	ENSP00000269571.4:p.His1104Gln
ENST00000269571.9:c.3312T>G	ENSP00000269571.4:p.His1104Gln
ENST00000406381.6:c.3222T>G	ENSP00000385185.2:p.His1074Gln
ENST00000445658.6:c.2484T>G	ENSP00000404047.2:p.His828Gln
ENST00000541774.5:c.3267T>G	ENSP00000446466.1:p.His1089Gln
ENST00000578373.5:c.*3102T>G	ENSP00000463427.1:n.*3102T>G
ENST00000584450.5:c.3160-242T>G	ENSP00000463714.1:n.3160-242T>G
ENST00000584601.5:c.3222T>G	ENSP00000462438.1:p.His1074Gln
NM_001005862.2:c.3222T>G , LRG_724t1:c.3222T>G	NP_001005862.1:p.His1074Gln
NM_001289936.1:c.3267T>G , LRG_724t4:c.3267T>G	NP_001276865.1:p.His1089Gln
NM_001289937.1:c.3160-242T>G	NP_001276866.1:n.3160-242T>G
NM_004448.3:c.3312T>G , LRG_724t2:c.3312T>G	NP_004439.2:p.His1104Gln
NR_110535.1:n.3636T>G
XM_024450641.1:c.3450T>G	XP_024306409.1:p.His1150Gln
XM_024450642.1:c.3405T>G	XP_024306410.1:p.His1135Gln
XM_024450643.1:c.3360T>G	XP_024306411.1:p.His1120Gln
NM_001005862.3:c.3222T>G	NP_001005862.1:p.His1074Gln
NM_001289936.2:c.3267T>G	NP_001276865.1:p.His1089Gln
NM_001289937.2:c.3160-242T>G	NP_001276866.1:n.3160-242T>G
NM_001382782.1:c.3222T>G	NP_001369711.1:p.His1074Gln
NM_001382783.1:c.3222T>G	NP_001369712.1:p.His1074Gln
NM_001382784.1:c.3429T>G	NP_001369713.1:p.His1143Gln
NM_001382785.1:c.3414T>G	NP_001369714.1:p.His1138Gln
NM_001382786.1:c.3393T>G	NP_001369715.1:p.His1131Gln
NM_001382787.1:c.3387T>G	NP_001369716.1:p.His1129Gln
NM_001382788.1:c.3342T>G	NP_001369717.1:p.His1114Gln
NM_001382789.1:c.3333T>G	NP_001369718.1:p.His1111Gln
NM_001382790.1:c.3309T>G	NP_001369719.1:p.His1103Gln
NM_001382791.1:c.3303T>G	NP_001369720.1:p.His1101Gln
NM_001382792.1:c.3276T>G	NP_001369721.1:p.His1092Gln
NM_001382793.1:c.3270T>G	NP_001369722.1:p.His1090Gln
NM_001382794.1:c.3270T>G	NP_001369723.1:p.His1090Gln
NM_001382795.1:c.3264T>G	NP_001369724.1:p.His1088Gln
NM_001382796.1:c.3225T>G	NP_001369725.1:p.His1075Gln
NM_001382797.1:c.3213T>G	NP_001369726.1:p.His1071Gln
NM_001382798.1:c.3156T>G	NP_001369727.1:p.His1052Gln
NM_001382799.1:c.3132T>G	NP_001369728.1:p.His1044Gln
NM_001382800.1:c.3126T>G	NP_001369729.1:p.His1042Gln
NM_001382801.1:c.3108T>G	NP_001369730.1:p.His1036Gln
NM_001382802.1:c.3054T>G	NP_001369731.1:p.His1018Gln
NM_001382803.1:c.3118-242T>G	NP_001369732.1:n.3118-242T>G
NM_001382804.1:c.2484T>G	NP_001369733.1:p.His828Gln
NM_001382805.1:c.2361T>G	NP_001369734.1:p.His787Gln
NM_001382806.1:c.2274T>G	NP_001369735.1:p.His758Gln
NM_004448.4:c.3312T>G MANE Select	NP_004439.2:p.His1104Gln
NR_110535.2:n.3550T>G