Canonical Allele Identifier: CA499890250

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143251925
• MyVariant Identifiers: chr17:g.37883721G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727468G>T , CM000679.2:g.39727468G>T	GRCh38
NC_000017.10:g.37883721G>T , CM000679.1:g.37883721G>T	GRCh37
NC_000017.9:g.35137247G>T	NCBI36
NG_007503.1:g.44329G>T , LRG_724:g.44329G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3333G>T MANE Select	ENSP00000269571.4:p.Arg1111=
ENST00000269571.9:c.3333G>T	ENSP00000269571.4:p.Arg1111=
ENST00000406381.6:c.3243G>T	ENSP00000385185.2:p.Arg1081=
ENST00000445658.6:c.2505G>T	ENSP00000404047.2:p.Arg835=
ENST00000541774.5:c.3288G>T	ENSP00000446466.1:p.Arg1096=
ENST00000578373.5:c.*3123G>T	ENSP00000463427.1:n.*3123G>T
ENST00000584450.5:c.3160-221G>T	ENSP00000463714.1:n.3160-221G>T
ENST00000584601.5:c.3243G>T	ENSP00000462438.1:p.Arg1081=
NM_001005862.2:c.3243G>T , LRG_724t1:c.3243G>T	NP_001005862.1:p.Arg1081=
NM_001289936.1:c.3288G>T , LRG_724t4:c.3288G>T	NP_001276865.1:p.Arg1096=
NM_001289937.1:c.3160-221G>T	NP_001276866.1:n.3160-221G>T
NM_004448.3:c.3333G>T , LRG_724t2:c.3333G>T	NP_004439.2:p.Arg1111=
NR_110535.1:n.3657G>T
XM_024450641.1:c.3471G>T	XP_024306409.1:p.Arg1157=
XM_024450642.1:c.3426G>T	XP_024306410.1:p.Arg1142=
XM_024450643.1:c.3381G>T	XP_024306411.1:p.Arg1127=
NM_001005862.3:c.3243G>T	NP_001005862.1:p.Arg1081=
NM_001289936.2:c.3288G>T	NP_001276865.1:p.Arg1096=
NM_001289937.2:c.3160-221G>T	NP_001276866.1:n.3160-221G>T
NM_001382782.1:c.3243G>T	NP_001369711.1:p.Arg1081=
NM_001382783.1:c.3243G>T	NP_001369712.1:p.Arg1081=
NM_001382784.1:c.3450G>T	NP_001369713.1:p.Arg1150=
NM_001382785.1:c.3435G>T	NP_001369714.1:p.Arg1145=
NM_001382786.1:c.3414G>T	NP_001369715.1:p.Arg1138=
NM_001382787.1:c.3408G>T	NP_001369716.1:p.Arg1136=
NM_001382788.1:c.3363G>T	NP_001369717.1:p.Arg1121=
NM_001382789.1:c.3354G>T	NP_001369718.1:p.Arg1118=
NM_001382790.1:c.3330G>T	NP_001369719.1:p.Arg1110=
NM_001382791.1:c.3324G>T	NP_001369720.1:p.Arg1108=
NM_001382792.1:c.3297G>T	NP_001369721.1:p.Arg1099=
NM_001382793.1:c.3291G>T	NP_001369722.1:p.Arg1097=
NM_001382794.1:c.3291G>T	NP_001369723.1:p.Arg1097=
NM_001382795.1:c.3285G>T	NP_001369724.1:p.Arg1095=
NM_001382796.1:c.3246G>T	NP_001369725.1:p.Arg1082=
NM_001382797.1:c.3234G>T	NP_001369726.1:p.Arg1078=
NM_001382798.1:c.3177G>T	NP_001369727.1:p.Arg1059=
NM_001382799.1:c.3153G>T	NP_001369728.1:p.Arg1051=
NM_001382800.1:c.3147G>T	NP_001369729.1:p.Arg1049=
NM_001382801.1:c.3129G>T	NP_001369730.1:p.Arg1043=
NM_001382802.1:c.3075G>T	NP_001369731.1:p.Arg1025=
NM_001382803.1:c.3118-221G>T	NP_001369732.1:n.3118-221G>T
NM_001382804.1:c.2505G>T	NP_001369733.1:p.Arg835=
NM_001382805.1:c.2382G>T	NP_001369734.1:p.Arg794=
NM_001382806.1:c.2295G>T	NP_001369735.1:p.Arg765=
NM_004448.4:c.3333G>T MANE Select	NP_004439.2:p.Arg1111=
NR_110535.2:n.3571G>T