Canonical Allele Identifier: CA499890281

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143257141
• MyVariant Identifiers: chr17:g.37883766C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727513C>T , CM000679.2:g.39727513C>T	GRCh38
NC_000017.10:g.37883766C>T , CM000679.1:g.37883766C>T	GRCh37
NC_000017.9:g.35137292C>T	NCBI36
NG_007503.1:g.44374C>T , LRG_724:g.44374C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3378C>T MANE Select	ENSP00000269571.4:p.Gly1126=
ENST00000269571.9:c.3378C>T	ENSP00000269571.4:p.Gly1126=
ENST00000406381.6:c.3288C>T	ENSP00000385185.2:p.Gly1096=
ENST00000445658.6:c.2550C>T	ENSP00000404047.2:p.Gly850=
ENST00000541774.5:c.3333C>T	ENSP00000446466.1:p.Gly1111=
ENST00000578373.5:c.*3168C>T	ENSP00000463427.1:n.*3168C>T
ENST00000584450.5:c.3160-176C>T	ENSP00000463714.1:n.3160-176C>T
ENST00000584601.5:c.3288C>T	ENSP00000462438.1:p.Gly1096=
NM_001005862.2:c.3288C>T , LRG_724t1:c.3288C>T	NP_001005862.1:p.Gly1096=
NM_001289936.1:c.3333C>T , LRG_724t4:c.3333C>T	NP_001276865.1:p.Gly1111=
NM_001289937.1:c.3160-176C>T	NP_001276866.1:n.3160-176C>T
NM_004448.3:c.3378C>T , LRG_724t2:c.3378C>T	NP_004439.2:p.Gly1126=
NR_110535.1:n.3702C>T
XM_024450641.1:c.3516C>T	XP_024306409.1:p.Gly1172=
XM_024450642.1:c.3471C>T	XP_024306410.1:p.Gly1157=
XM_024450643.1:c.3426C>T	XP_024306411.1:p.Gly1142=
NM_001005862.3:c.3288C>T	NP_001005862.1:p.Gly1096=
NM_001289936.2:c.3333C>T	NP_001276865.1:p.Gly1111=
NM_001289937.2:c.3160-176C>T	NP_001276866.1:n.3160-176C>T
NM_001382782.1:c.3288C>T	NP_001369711.1:p.Gly1096=
NM_001382783.1:c.3288C>T	NP_001369712.1:p.Gly1096=
NM_001382784.1:c.3495C>T	NP_001369713.1:p.Gly1165=
NM_001382785.1:c.3480C>T	NP_001369714.1:p.Gly1160=
NM_001382786.1:c.3459C>T	NP_001369715.1:p.Gly1153=
NM_001382787.1:c.3453C>T	NP_001369716.1:p.Gly1151=
NM_001382788.1:c.3408C>T	NP_001369717.1:p.Gly1136=
NM_001382789.1:c.3399C>T	NP_001369718.1:p.Gly1133=
NM_001382790.1:c.3375C>T	NP_001369719.1:p.Gly1125=
NM_001382791.1:c.3369C>T	NP_001369720.1:p.Gly1123=
NM_001382792.1:c.3342C>T	NP_001369721.1:p.Gly1114=
NM_001382793.1:c.3336C>T	NP_001369722.1:p.Gly1112=
NM_001382794.1:c.3336C>T	NP_001369723.1:p.Gly1112=
NM_001382795.1:c.3330C>T	NP_001369724.1:p.Gly1110=
NM_001382796.1:c.3291C>T	NP_001369725.1:p.Gly1097=
NM_001382797.1:c.3279C>T	NP_001369726.1:p.Gly1093=
NM_001382798.1:c.3222C>T	NP_001369727.1:p.Gly1074=
NM_001382799.1:c.3198C>T	NP_001369728.1:p.Gly1066=
NM_001382800.1:c.3192C>T	NP_001369729.1:p.Gly1064=
NM_001382801.1:c.3174C>T	NP_001369730.1:p.Gly1058=
NM_001382802.1:c.3120C>T	NP_001369731.1:p.Gly1040=
NM_001382803.1:c.3118-176C>T	NP_001369732.1:n.3118-176C>T
NM_001382804.1:c.2550C>T	NP_001369733.1:p.Gly850=
NM_001382805.1:c.2427C>T	NP_001369734.1:p.Gly809=
NM_001382806.1:c.2340C>T	NP_001369735.1:p.Gly780=
NM_004448.4:c.3378C>T MANE Select	NP_004439.2:p.Gly1126=
NR_110535.2:n.3616C>T