Canonical Allele Identifier: CA499890742

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143302954
• MyVariant Identifiers: chr17:g.37884096T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727843T>A , CM000679.2:g.39727843T>A	GRCh38
NC_000017.10:g.37884096T>A , CM000679.1:g.37884096T>A	GRCh37
NC_000017.9:g.35137622T>A	NCBI36
NG_007503.1:g.44704T>A , LRG_724:g.44704T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3567T>A MANE Select	ENSP00000269571.4:p.Gly1189=
ENST00000269571.9:c.3567T>A	ENSP00000269571.4:p.Gly1189=
ENST00000406381.6:c.3477T>A	ENSP00000385185.2:p.Gly1159=
ENST00000445658.6:c.2739T>A	ENSP00000404047.2:p.Gly913=
ENST00000541774.5:c.3522T>A	ENSP00000446466.1:p.Gly1174=
ENST00000578373.5:c.*3357T>A	ENSP00000463427.1:n.*3357T>A
ENST00000584450.5:c.*146T>A	ENSP00000463714.1:n.*146T>A
ENST00000584601.5:c.3477T>A	ENSP00000462438.1:p.Gly1159=
NM_001005862.2:c.3477T>A , LRG_724t1:c.3477T>A	NP_001005862.1:p.Gly1159=
NM_001289936.1:c.3522T>A , LRG_724t4:c.3522T>A	NP_001276865.1:p.Gly1174=
NM_001289937.1:c.*146T>A	NP_001276866.1:n.*146T>A
NM_004448.3:c.3567T>A , LRG_724t2:c.3567T>A	NP_004439.2:p.Gly1189=
NR_110535.1:n.3891T>A
XM_024450641.1:c.3705T>A	XP_024306409.1:p.Gly1235=
XM_024450642.1:c.3660T>A	XP_024306410.1:p.Gly1220=
XM_024450643.1:c.3615T>A	XP_024306411.1:p.Gly1205=
NM_001005862.3:c.3477T>A	NP_001005862.1:p.Gly1159=
NM_001289936.2:c.3522T>A	NP_001276865.1:p.Gly1174=
NM_001289937.2:c.*146T>A	NP_001276866.1:n.*146T>A
NM_001382782.1:c.3477T>A	NP_001369711.1:p.Gly1159=
NM_001382783.1:c.3477T>A	NP_001369712.1:p.Gly1159=
NM_001382784.1:c.3684T>A	NP_001369713.1:p.Gly1228=
NM_001382785.1:c.3669T>A	NP_001369714.1:p.Gly1223=
NM_001382786.1:c.3648T>A	NP_001369715.1:p.Gly1216=
NM_001382787.1:c.3642T>A	NP_001369716.1:p.Gly1214=
NM_001382788.1:c.3597T>A	NP_001369717.1:p.Gly1199=
NM_001382789.1:c.3588T>A	NP_001369718.1:p.Gly1196=
NM_001382790.1:c.3564T>A	NP_001369719.1:p.Gly1188=
NM_001382791.1:c.3558T>A	NP_001369720.1:p.Gly1186=
NM_001382792.1:c.3531T>A	NP_001369721.1:p.Gly1177=
NM_001382793.1:c.3525T>A	NP_001369722.1:p.Gly1175=
NM_001382794.1:c.3525T>A	NP_001369723.1:p.Gly1175=
NM_001382795.1:c.3519T>A	NP_001369724.1:p.Gly1173=
NM_001382796.1:c.3480T>A	NP_001369725.1:p.Gly1160=
NM_001382797.1:c.3468T>A	NP_001369726.1:p.Gly1156=
NM_001382798.1:c.3411T>A	NP_001369727.1:p.Gly1137=
NM_001382799.1:c.3387T>A	NP_001369728.1:p.Gly1129=
NM_001382800.1:c.3381T>A	NP_001369729.1:p.Gly1127=
NM_001382801.1:c.3363T>A	NP_001369730.1:p.Gly1121=
NM_001382802.1:c.3309T>A	NP_001369731.1:p.Gly1103=
NM_001382803.1:c.*146T>A	NP_001369732.1:n.*146T>A
NM_001382804.1:c.2739T>A	NP_001369733.1:p.Gly913=
NM_001382805.1:c.2616T>A	NP_001369734.1:p.Gly872=
NM_001382806.1:c.2529T>A	NP_001369735.1:p.Gly843=
NM_004448.4:c.3567T>A MANE Select	NP_004439.2:p.Gly1189=
NR_110535.2:n.3805T>A