Canonical Allele Identifier: CA499671672

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143248275
• MyVariant Identifiers: chr17:g.37883688C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727435C>T , CM000679.2:g.39727435C>T	GRCh38
NC_000017.10:g.37883688C>T , CM000679.1:g.37883688C>T	GRCh37
NC_000017.9:g.35137214C>T	NCBI36
NG_007503.1:g.44296C>T , LRG_724:g.44296C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3300C>T MANE Select	ENSP00000269571.4:p.Ser1100=
ENST00000269571.9:c.3300C>T	ENSP00000269571.4:p.Ser1100=
ENST00000406381.6:c.3210C>T	ENSP00000385185.2:p.Ser1070=
ENST00000445658.6:c.2472C>T	ENSP00000404047.2:p.Ser824=
ENST00000541774.5:c.3255C>T	ENSP00000446466.1:p.Ser1085=
ENST00000578373.5:c.*3090C>T	ENSP00000463427.1:n.*3090C>T
ENST00000584450.5:c.3160-254C>T	ENSP00000463714.1:n.3160-254C>T
ENST00000584601.5:c.3210C>T	ENSP00000462438.1:p.Ser1070=
NM_001005862.2:c.3210C>T , LRG_724t1:c.3210C>T	NP_001005862.1:p.Ser1070=
NM_001289936.1:c.3255C>T , LRG_724t4:c.3255C>T	NP_001276865.1:p.Ser1085=
NM_001289937.1:c.3160-254C>T	NP_001276866.1:n.3160-254C>T
NM_004448.3:c.3300C>T , LRG_724t2:c.3300C>T	NP_004439.2:p.Ser1100=
NR_110535.1:n.3624C>T
XM_024450641.1:c.3438C>T	XP_024306409.1:p.Ser1146=
XM_024450642.1:c.3393C>T	XP_024306410.1:p.Ser1131=
XM_024450643.1:c.3348C>T	XP_024306411.1:p.Ser1116=
NM_001005862.3:c.3210C>T	NP_001005862.1:p.Ser1070=
NM_001289936.2:c.3255C>T	NP_001276865.1:p.Ser1085=
NM_001289937.2:c.3160-254C>T	NP_001276866.1:n.3160-254C>T
NM_001382782.1:c.3210C>T	NP_001369711.1:p.Ser1070=
NM_001382783.1:c.3210C>T	NP_001369712.1:p.Ser1070=
NM_001382784.1:c.3417C>T	NP_001369713.1:p.Ser1139=
NM_001382785.1:c.3402C>T	NP_001369714.1:p.Ser1134=
NM_001382786.1:c.3381C>T	NP_001369715.1:p.Ser1127=
NM_001382787.1:c.3375C>T	NP_001369716.1:p.Ser1125=
NM_001382788.1:c.3330C>T	NP_001369717.1:p.Ser1110=
NM_001382789.1:c.3321C>T	NP_001369718.1:p.Ser1107=
NM_001382790.1:c.3297C>T	NP_001369719.1:p.Ser1099=
NM_001382791.1:c.3291C>T	NP_001369720.1:p.Ser1097=
NM_001382792.1:c.3264C>T	NP_001369721.1:p.Ser1088=
NM_001382793.1:c.3258C>T	NP_001369722.1:p.Ser1086=
NM_001382794.1:c.3258C>T	NP_001369723.1:p.Ser1086=
NM_001382795.1:c.3252C>T	NP_001369724.1:p.Ser1084=
NM_001382796.1:c.3213C>T	NP_001369725.1:p.Ser1071=
NM_001382797.1:c.3201C>T	NP_001369726.1:p.Ser1067=
NM_001382798.1:c.3144C>T	NP_001369727.1:p.Ser1048=
NM_001382799.1:c.3120C>T	NP_001369728.1:p.Ser1040=
NM_001382800.1:c.3114C>T	NP_001369729.1:p.Ser1038=
NM_001382801.1:c.3096C>T	NP_001369730.1:p.Ser1032=
NM_001382802.1:c.3042C>T	NP_001369731.1:p.Ser1014=
NM_001382803.1:c.3118-254C>T	NP_001369732.1:n.3118-254C>T
NM_001382804.1:c.2472C>T	NP_001369733.1:p.Ser824=
NM_001382805.1:c.2349C>T	NP_001369734.1:p.Ser783=
NM_001382806.1:c.2262C>T	NP_001369735.1:p.Ser754=
NM_004448.4:c.3300C>T MANE Select	NP_004439.2:p.Ser1100=
NR_110535.2:n.3538C>T