Canonical Allele Identifier: CA499890631

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143294658
• MyVariant Identifiers: chr17:g.37884021T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727768T>G , CM000679.2:g.39727768T>G	GRCh38
NC_000017.10:g.37884021T>G , CM000679.1:g.37884021T>G	GRCh37
NC_000017.9:g.35137547T>G	NCBI36
NG_007503.1:g.44629T>G , LRG_724:g.44629T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3492T>G MANE Select	ENSP00000269571.4:p.Gly1164=
ENST00000269571.9:c.3492T>G	ENSP00000269571.4:p.Gly1164=
ENST00000406381.6:c.3402T>G	ENSP00000385185.2:p.Gly1134=
ENST00000445658.6:c.2664T>G	ENSP00000404047.2:p.Gly888=
ENST00000541774.5:c.3447T>G	ENSP00000446466.1:p.Gly1149=
ENST00000578373.5:c.*3282T>G	ENSP00000463427.1:n.*3282T>G
ENST00000584450.5:c.*71T>G	ENSP00000463714.1:n.*71T>G
ENST00000584601.5:c.3402T>G	ENSP00000462438.1:p.Gly1134=
NM_001005862.2:c.3402T>G , LRG_724t1:c.3402T>G	NP_001005862.1:p.Gly1134=
NM_001289936.1:c.3447T>G , LRG_724t4:c.3447T>G	NP_001276865.1:p.Gly1149=
NM_001289937.1:c.*71T>G	NP_001276866.1:n.*71T>G
NM_004448.3:c.3492T>G , LRG_724t2:c.3492T>G	NP_004439.2:p.Gly1164=
NR_110535.1:n.3816T>G
XM_024450641.1:c.3630T>G	XP_024306409.1:p.Gly1210=
XM_024450642.1:c.3585T>G	XP_024306410.1:p.Gly1195=
XM_024450643.1:c.3540T>G	XP_024306411.1:p.Gly1180=
NM_001005862.3:c.3402T>G	NP_001005862.1:p.Gly1134=
NM_001289936.2:c.3447T>G	NP_001276865.1:p.Gly1149=
NM_001289937.2:c.*71T>G	NP_001276866.1:n.*71T>G
NM_001382782.1:c.3402T>G	NP_001369711.1:p.Gly1134=
NM_001382783.1:c.3402T>G	NP_001369712.1:p.Gly1134=
NM_001382784.1:c.3609T>G	NP_001369713.1:p.Gly1203=
NM_001382785.1:c.3594T>G	NP_001369714.1:p.Gly1198=
NM_001382786.1:c.3573T>G	NP_001369715.1:p.Gly1191=
NM_001382787.1:c.3567T>G	NP_001369716.1:p.Gly1189=
NM_001382788.1:c.3522T>G	NP_001369717.1:p.Gly1174=
NM_001382789.1:c.3513T>G	NP_001369718.1:p.Gly1171=
NM_001382790.1:c.3489T>G	NP_001369719.1:p.Gly1163=
NM_001382791.1:c.3483T>G	NP_001369720.1:p.Gly1161=
NM_001382792.1:c.3456T>G	NP_001369721.1:p.Gly1152=
NM_001382793.1:c.3450T>G	NP_001369722.1:p.Gly1150=
NM_001382794.1:c.3450T>G	NP_001369723.1:p.Gly1150=
NM_001382795.1:c.3444T>G	NP_001369724.1:p.Gly1148=
NM_001382796.1:c.3405T>G	NP_001369725.1:p.Gly1135=
NM_001382797.1:c.3393T>G	NP_001369726.1:p.Gly1131=
NM_001382798.1:c.3336T>G	NP_001369727.1:p.Gly1112=
NM_001382799.1:c.3312T>G	NP_001369728.1:p.Gly1104=
NM_001382800.1:c.3306T>G	NP_001369729.1:p.Gly1102=
NM_001382801.1:c.3288T>G	NP_001369730.1:p.Gly1096=
NM_001382802.1:c.3234T>G	NP_001369731.1:p.Gly1078=
NM_001382803.1:c.*71T>G	NP_001369732.1:n.*71T>G
NM_001382804.1:c.2664T>G	NP_001369733.1:p.Gly888=
NM_001382805.1:c.2541T>G	NP_001369734.1:p.Gly847=
NM_001382806.1:c.2454T>G	NP_001369735.1:p.Gly818=
NM_004448.4:c.3492T>G MANE Select	NP_004439.2:p.Gly1164=
NR_110535.2:n.3730T>G