Canonical Allele Identifier: CA499890738

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143302641
• MyVariant Identifiers: chr17:g.37884093G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727840G>T , CM000679.2:g.39727840G>T	GRCh38
NC_000017.10:g.37884093G>T , CM000679.1:g.37884093G>T	GRCh37
NC_000017.9:g.35137619G>T	NCBI36
NG_007503.1:g.44701G>T , LRG_724:g.44701G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3564G>T MANE Select	ENSP00000269571.4:p.Gly1188=
ENST00000269571.9:c.3564G>T	ENSP00000269571.4:p.Gly1188=
ENST00000406381.6:c.3474G>T	ENSP00000385185.2:p.Gly1158=
ENST00000445658.6:c.2736G>T	ENSP00000404047.2:p.Gly912=
ENST00000541774.5:c.3519G>T	ENSP00000446466.1:p.Gly1173=
ENST00000578373.5:c.*3354G>T	ENSP00000463427.1:n.*3354G>T
ENST00000584450.5:c.*143G>T	ENSP00000463714.1:n.*143G>T
ENST00000584601.5:c.3474G>T	ENSP00000462438.1:p.Gly1158=
NM_001005862.2:c.3474G>T , LRG_724t1:c.3474G>T	NP_001005862.1:p.Gly1158=
NM_001289936.1:c.3519G>T , LRG_724t4:c.3519G>T	NP_001276865.1:p.Gly1173=
NM_001289937.1:c.*143G>T	NP_001276866.1:n.*143G>T
NM_004448.3:c.3564G>T , LRG_724t2:c.3564G>T	NP_004439.2:p.Gly1188=
NR_110535.1:n.3888G>T
XM_024450641.1:c.3702G>T	XP_024306409.1:p.Gly1234=
XM_024450642.1:c.3657G>T	XP_024306410.1:p.Gly1219=
XM_024450643.1:c.3612G>T	XP_024306411.1:p.Gly1204=
NM_001005862.3:c.3474G>T	NP_001005862.1:p.Gly1158=
NM_001289936.2:c.3519G>T	NP_001276865.1:p.Gly1173=
NM_001289937.2:c.*143G>T	NP_001276866.1:n.*143G>T
NM_001382782.1:c.3474G>T	NP_001369711.1:p.Gly1158=
NM_001382783.1:c.3474G>T	NP_001369712.1:p.Gly1158=
NM_001382784.1:c.3681G>T	NP_001369713.1:p.Gly1227=
NM_001382785.1:c.3666G>T	NP_001369714.1:p.Gly1222=
NM_001382786.1:c.3645G>T	NP_001369715.1:p.Gly1215=
NM_001382787.1:c.3639G>T	NP_001369716.1:p.Gly1213=
NM_001382788.1:c.3594G>T	NP_001369717.1:p.Gly1198=
NM_001382789.1:c.3585G>T	NP_001369718.1:p.Gly1195=
NM_001382790.1:c.3561G>T	NP_001369719.1:p.Gly1187=
NM_001382791.1:c.3555G>T	NP_001369720.1:p.Gly1185=
NM_001382792.1:c.3528G>T	NP_001369721.1:p.Gly1176=
NM_001382793.1:c.3522G>T	NP_001369722.1:p.Gly1174=
NM_001382794.1:c.3522G>T	NP_001369723.1:p.Gly1174=
NM_001382795.1:c.3516G>T	NP_001369724.1:p.Gly1172=
NM_001382796.1:c.3477G>T	NP_001369725.1:p.Gly1159=
NM_001382797.1:c.3465G>T	NP_001369726.1:p.Gly1155=
NM_001382798.1:c.3408G>T	NP_001369727.1:p.Gly1136=
NM_001382799.1:c.3384G>T	NP_001369728.1:p.Gly1128=
NM_001382800.1:c.3378G>T	NP_001369729.1:p.Gly1126=
NM_001382801.1:c.3360G>T	NP_001369730.1:p.Gly1120=
NM_001382802.1:c.3306G>T	NP_001369731.1:p.Gly1102=
NM_001382803.1:c.*143G>T	NP_001369732.1:n.*143G>T
NM_001382804.1:c.2736G>T	NP_001369733.1:p.Gly912=
NM_001382805.1:c.2613G>T	NP_001369734.1:p.Gly871=
NM_001382806.1:c.2526G>T	NP_001369735.1:p.Gly842=
NM_004448.4:c.3564G>T MANE Select	NP_004439.2:p.Gly1188=
NR_110535.2:n.3802G>T