Canonical Allele Identifier: CA399314593

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143315801
• gnomAD v4: 17-39727968-G-T
• MyVariant Identifiers: chr17:g.37884221G>T (hg19) ; chr17:g.39727968G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727968G>T , CM000679.2:g.39727968G>T	GRCh38
NC_000017.10:g.37884221G>T , CM000679.1:g.37884221G>T	GRCh37
NC_000017.9:g.35137747G>T	NCBI36
NG_007503.1:g.44829G>T , LRG_724:g.44829G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3692G>T MANE Select	ENSP00000269571.4:p.Gly1231Val
ENST00000269571.9:c.3692G>T	ENSP00000269571.4:p.Gly1231Val
ENST00000406381.6:c.3602G>T	ENSP00000385185.2:p.Gly1201Val
ENST00000445658.6:c.2864G>T	ENSP00000404047.2:p.Gly955Val
ENST00000541774.5:c.3647G>T	ENSP00000446466.1:p.Gly1216Val
ENST00000578373.5:c.*3482G>T	ENSP00000463427.1:n.*3482G>T
ENST00000584450.5:c.*271G>T	ENSP00000463714.1:n.*271G>T
ENST00000584601.5:c.3602G>T	ENSP00000462438.1:p.Gly1201Val
NM_001005862.2:c.3602G>T , LRG_724t1:c.3602G>T	NP_001005862.1:p.Gly1201Val
NM_001289936.1:c.3647G>T , LRG_724t4:c.3647G>T	NP_001276865.1:p.Gly1216Val
NM_001289937.1:c.*271G>T	NP_001276866.1:n.*271G>T
NM_004448.3:c.3692G>T , LRG_724t2:c.3692G>T	NP_004439.2:p.Gly1231Val
NR_110535.1:n.4016G>T
XM_024450641.1:c.3830G>T	XP_024306409.1:p.Gly1277Val
XM_024450642.1:c.3785G>T	XP_024306410.1:p.Gly1262Val
XM_024450643.1:c.3740G>T	XP_024306411.1:p.Gly1247Val
NM_001005862.3:c.3602G>T	NP_001005862.1:p.Gly1201Val
NM_001289936.2:c.3647G>T	NP_001276865.1:p.Gly1216Val
NM_001289937.2:c.*271G>T	NP_001276866.1:n.*271G>T
NM_001382782.1:c.3602G>T	NP_001369711.1:p.Gly1201Val
NM_001382783.1:c.3602G>T	NP_001369712.1:p.Gly1201Val
NM_001382784.1:c.3809G>T	NP_001369713.1:p.Gly1270Val
NM_001382785.1:c.3794G>T	NP_001369714.1:p.Gly1265Val
NM_001382786.1:c.3773G>T	NP_001369715.1:p.Gly1258Val
NM_001382787.1:c.3767G>T	NP_001369716.1:p.Gly1256Val
NM_001382788.1:c.3722G>T	NP_001369717.1:p.Gly1241Val
NM_001382789.1:c.3713G>T	NP_001369718.1:p.Gly1238Val
NM_001382790.1:c.3689G>T	NP_001369719.1:p.Gly1230Val
NM_001382791.1:c.3683G>T	NP_001369720.1:p.Gly1228Val
NM_001382792.1:c.3656G>T	NP_001369721.1:p.Gly1219Val
NM_001382793.1:c.3650G>T	NP_001369722.1:p.Gly1217Val
NM_001382794.1:c.3650G>T	NP_001369723.1:p.Gly1217Val
NM_001382795.1:c.3644G>T	NP_001369724.1:p.Gly1215Val
NM_001382796.1:c.3605G>T	NP_001369725.1:p.Gly1202Val
NM_001382797.1:c.3593G>T	NP_001369726.1:p.Gly1198Val
NM_001382798.1:c.3536G>T	NP_001369727.1:p.Gly1179Val
NM_001382799.1:c.3512G>T	NP_001369728.1:p.Gly1171Val
NM_001382800.1:c.3506G>T	NP_001369729.1:p.Gly1169Val
NM_001382801.1:c.3488G>T	NP_001369730.1:p.Gly1163Val
NM_001382802.1:c.3434G>T	NP_001369731.1:p.Gly1145Val
NM_001382803.1:c.*271G>T	NP_001369732.1:n.*271G>T
NM_001382804.1:c.2864G>T	NP_001369733.1:p.Gly955Val
NM_001382805.1:c.2741G>T	NP_001369734.1:p.Gly914Val
NM_001382806.1:c.2654G>T	NP_001369735.1:p.Gly885Val
NM_004448.4:c.3692G>T MANE Select	NP_004439.2:p.Gly1231Val
NR_110535.2:n.3930G>T