Canonical Allele Identifier: CA499890868

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143313331
• MyVariant Identifiers: chr17:g.37884195C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727942C>T , CM000679.2:g.39727942C>T	GRCh38
NC_000017.10:g.37884195C>T , CM000679.1:g.37884195C>T	GRCh37
NC_000017.9:g.35137721C>T	NCBI36
NG_007503.1:g.44803C>T , LRG_724:g.44803C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3666C>T MANE Select	ENSP00000269571.4:p.Tyr1222=
ENST00000269571.9:c.3666C>T	ENSP00000269571.4:p.Tyr1222=
ENST00000406381.6:c.3576C>T	ENSP00000385185.2:p.Tyr1192=
ENST00000445658.6:c.2838C>T	ENSP00000404047.2:p.Tyr946=
ENST00000541774.5:c.3621C>T	ENSP00000446466.1:p.Tyr1207=
ENST00000578373.5:c.*3456C>T	ENSP00000463427.1:n.*3456C>T
ENST00000584450.5:c.*245C>T	ENSP00000463714.1:n.*245C>T
ENST00000584601.5:c.3576C>T	ENSP00000462438.1:p.Tyr1192=
NM_001005862.2:c.3576C>T , LRG_724t1:c.3576C>T	NP_001005862.1:p.Tyr1192=
NM_001289936.1:c.3621C>T , LRG_724t4:c.3621C>T	NP_001276865.1:p.Tyr1207=
NM_001289937.1:c.*245C>T	NP_001276866.1:n.*245C>T
NM_004448.3:c.3666C>T , LRG_724t2:c.3666C>T	NP_004439.2:p.Tyr1222=
NR_110535.1:n.3990C>T
XM_024450641.1:c.3804C>T	XP_024306409.1:p.Tyr1268=
XM_024450642.1:c.3759C>T	XP_024306410.1:p.Tyr1253=
XM_024450643.1:c.3714C>T	XP_024306411.1:p.Tyr1238=
NM_001005862.3:c.3576C>T	NP_001005862.1:p.Tyr1192=
NM_001289936.2:c.3621C>T	NP_001276865.1:p.Tyr1207=
NM_001289937.2:c.*245C>T	NP_001276866.1:n.*245C>T
NM_001382782.1:c.3576C>T	NP_001369711.1:p.Tyr1192=
NM_001382783.1:c.3576C>T	NP_001369712.1:p.Tyr1192=
NM_001382784.1:c.3783C>T	NP_001369713.1:p.Tyr1261=
NM_001382785.1:c.3768C>T	NP_001369714.1:p.Tyr1256=
NM_001382786.1:c.3747C>T	NP_001369715.1:p.Tyr1249=
NM_001382787.1:c.3741C>T	NP_001369716.1:p.Tyr1247=
NM_001382788.1:c.3696C>T	NP_001369717.1:p.Tyr1232=
NM_001382789.1:c.3687C>T	NP_001369718.1:p.Tyr1229=
NM_001382790.1:c.3663C>T	NP_001369719.1:p.Tyr1221=
NM_001382791.1:c.3657C>T	NP_001369720.1:p.Tyr1219=
NM_001382792.1:c.3630C>T	NP_001369721.1:p.Tyr1210=
NM_001382793.1:c.3624C>T	NP_001369722.1:p.Tyr1208=
NM_001382794.1:c.3624C>T	NP_001369723.1:p.Tyr1208=
NM_001382795.1:c.3618C>T	NP_001369724.1:p.Tyr1206=
NM_001382796.1:c.3579C>T	NP_001369725.1:p.Tyr1193=
NM_001382797.1:c.3567C>T	NP_001369726.1:p.Tyr1189=
NM_001382798.1:c.3510C>T	NP_001369727.1:p.Tyr1170=
NM_001382799.1:c.3486C>T	NP_001369728.1:p.Tyr1162=
NM_001382800.1:c.3480C>T	NP_001369729.1:p.Tyr1160=
NM_001382801.1:c.3462C>T	NP_001369730.1:p.Tyr1154=
NM_001382802.1:c.3408C>T	NP_001369731.1:p.Tyr1136=
NM_001382803.1:c.*245C>T	NP_001369732.1:n.*245C>T
NM_001382804.1:c.2838C>T	NP_001369733.1:p.Tyr946=
NM_001382805.1:c.2715C>T	NP_001369734.1:p.Tyr905=
NM_001382806.1:c.2628C>T	NP_001369735.1:p.Tyr876=
NM_004448.4:c.3666C>T MANE Select	NP_004439.2:p.Tyr1222=
NR_110535.2:n.3904C>T