Canonical Allele Identifier: CA499890694

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143297617
• MyVariant Identifiers: chr17:g.37884051C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727798C>G , CM000679.2:g.39727798C>G	GRCh38
NC_000017.10:g.37884051C>G , CM000679.1:g.37884051C>G	GRCh37
NC_000017.9:g.35137577C>G	NCBI36
NG_007503.1:g.44659C>G , LRG_724:g.44659C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.3522C>G MANE Select	ENSP00000269571.4:p.Ser1174=
ENST00000269571.9:c.3522C>G	ENSP00000269571.4:p.Ser1174=
ENST00000406381.6:c.3432C>G	ENSP00000385185.2:p.Ser1144=
ENST00000445658.6:c.2694C>G	ENSP00000404047.2:p.Ser898=
ENST00000541774.5:c.3477C>G	ENSP00000446466.1:p.Ser1159=
ENST00000578373.5:c.*3312C>G	ENSP00000463427.1:n.*3312C>G
ENST00000584450.5:c.*101C>G	ENSP00000463714.1:n.*101C>G
ENST00000584601.5:c.3432C>G	ENSP00000462438.1:p.Ser1144=
NM_001005862.2:c.3432C>G , LRG_724t1:c.3432C>G	NP_001005862.1:p.Ser1144=
NM_001289936.1:c.3477C>G , LRG_724t4:c.3477C>G	NP_001276865.1:p.Ser1159=
NM_001289937.1:c.*101C>G	NP_001276866.1:n.*101C>G
NM_004448.3:c.3522C>G , LRG_724t2:c.3522C>G	NP_004439.2:p.Ser1174=
NR_110535.1:n.3846C>G
XM_024450641.1:c.3660C>G	XP_024306409.1:p.Ser1220=
XM_024450642.1:c.3615C>G	XP_024306410.1:p.Ser1205=
XM_024450643.1:c.3570C>G	XP_024306411.1:p.Ser1190=
NM_001005862.3:c.3432C>G	NP_001005862.1:p.Ser1144=
NM_001289936.2:c.3477C>G	NP_001276865.1:p.Ser1159=
NM_001289937.2:c.*101C>G	NP_001276866.1:n.*101C>G
NM_001382782.1:c.3432C>G	NP_001369711.1:p.Ser1144=
NM_001382783.1:c.3432C>G	NP_001369712.1:p.Ser1144=
NM_001382784.1:c.3639C>G	NP_001369713.1:p.Ser1213=
NM_001382785.1:c.3624C>G	NP_001369714.1:p.Ser1208=
NM_001382786.1:c.3603C>G	NP_001369715.1:p.Ser1201=
NM_001382787.1:c.3597C>G	NP_001369716.1:p.Ser1199=
NM_001382788.1:c.3552C>G	NP_001369717.1:p.Ser1184=
NM_001382789.1:c.3543C>G	NP_001369718.1:p.Ser1181=
NM_001382790.1:c.3519C>G	NP_001369719.1:p.Ser1173=
NM_001382791.1:c.3513C>G	NP_001369720.1:p.Ser1171=
NM_001382792.1:c.3486C>G	NP_001369721.1:p.Ser1162=
NM_001382793.1:c.3480C>G	NP_001369722.1:p.Ser1160=
NM_001382794.1:c.3480C>G	NP_001369723.1:p.Ser1160=
NM_001382795.1:c.3474C>G	NP_001369724.1:p.Ser1158=
NM_001382796.1:c.3435C>G	NP_001369725.1:p.Ser1145=
NM_001382797.1:c.3423C>G	NP_001369726.1:p.Ser1141=
NM_001382798.1:c.3366C>G	NP_001369727.1:p.Ser1122=
NM_001382799.1:c.3342C>G	NP_001369728.1:p.Ser1114=
NM_001382800.1:c.3336C>G	NP_001369729.1:p.Ser1112=
NM_001382801.1:c.3318C>G	NP_001369730.1:p.Ser1106=
NM_001382802.1:c.3264C>G	NP_001369731.1:p.Ser1088=
NM_001382803.1:c.*101C>G	NP_001369732.1:n.*101C>G
NM_001382804.1:c.2694C>G	NP_001369733.1:p.Ser898=
NM_001382805.1:c.2571C>G	NP_001369734.1:p.Ser857=
NM_001382806.1:c.2484C>G	NP_001369735.1:p.Ser828=
NM_004448.4:c.3522C>G MANE Select	NP_004439.2:p.Ser1174=
NR_110535.2:n.3760C>G