Canonical Allele Identifier: CA499890800

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143307568
• MyVariant Identifiers: chr17:g.37884138T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727885T>G , CM000679.2:g.39727885T>G	GRCh38
NC_000017.10:g.37884138T>G , CM000679.1:g.37884138T>G	GRCh37
NC_000017.9:g.35137664T>G	NCBI36
NG_007503.1:g.44746T>G , LRG_724:g.44746T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3609T>G MANE Select	ENSP00000269571.4:p.Ala1203=
ENST00000269571.9:c.3609T>G	ENSP00000269571.4:p.Ala1203=
ENST00000406381.6:c.3519T>G	ENSP00000385185.2:p.Ala1173=
ENST00000445658.6:c.2781T>G	ENSP00000404047.2:p.Ala927=
ENST00000541774.5:c.3564T>G	ENSP00000446466.1:p.Ala1188=
ENST00000578373.5:c.*3399T>G	ENSP00000463427.1:n.*3399T>G
ENST00000584450.5:c.*188T>G	ENSP00000463714.1:n.*188T>G
ENST00000584601.5:c.3519T>G	ENSP00000462438.1:p.Ala1173=
NM_001005862.2:c.3519T>G , LRG_724t1:c.3519T>G	NP_001005862.1:p.Ala1173=
NM_001289936.1:c.3564T>G , LRG_724t4:c.3564T>G	NP_001276865.1:p.Ala1188=
NM_001289937.1:c.*188T>G	NP_001276866.1:n.*188T>G
NM_004448.3:c.3609T>G , LRG_724t2:c.3609T>G	NP_004439.2:p.Ala1203=
NR_110535.1:n.3933T>G
XM_024450641.1:c.3747T>G	XP_024306409.1:p.Ala1249=
XM_024450642.1:c.3702T>G	XP_024306410.1:p.Ala1234=
XM_024450643.1:c.3657T>G	XP_024306411.1:p.Ala1219=
NM_001005862.3:c.3519T>G	NP_001005862.1:p.Ala1173=
NM_001289936.2:c.3564T>G	NP_001276865.1:p.Ala1188=
NM_001289937.2:c.*188T>G	NP_001276866.1:n.*188T>G
NM_001382782.1:c.3519T>G	NP_001369711.1:p.Ala1173=
NM_001382783.1:c.3519T>G	NP_001369712.1:p.Ala1173=
NM_001382784.1:c.3726T>G	NP_001369713.1:p.Ala1242=
NM_001382785.1:c.3711T>G	NP_001369714.1:p.Ala1237=
NM_001382786.1:c.3690T>G	NP_001369715.1:p.Ala1230=
NM_001382787.1:c.3684T>G	NP_001369716.1:p.Ala1228=
NM_001382788.1:c.3639T>G	NP_001369717.1:p.Ala1213=
NM_001382789.1:c.3630T>G	NP_001369718.1:p.Ala1210=
NM_001382790.1:c.3606T>G	NP_001369719.1:p.Ala1202=
NM_001382791.1:c.3600T>G	NP_001369720.1:p.Ala1200=
NM_001382792.1:c.3573T>G	NP_001369721.1:p.Ala1191=
NM_001382793.1:c.3567T>G	NP_001369722.1:p.Ala1189=
NM_001382794.1:c.3567T>G	NP_001369723.1:p.Ala1189=
NM_001382795.1:c.3561T>G	NP_001369724.1:p.Ala1187=
NM_001382796.1:c.3522T>G	NP_001369725.1:p.Ala1174=
NM_001382797.1:c.3510T>G	NP_001369726.1:p.Ala1170=
NM_001382798.1:c.3453T>G	NP_001369727.1:p.Ala1151=
NM_001382799.1:c.3429T>G	NP_001369728.1:p.Ala1143=
NM_001382800.1:c.3423T>G	NP_001369729.1:p.Ala1141=
NM_001382801.1:c.3405T>G	NP_001369730.1:p.Ala1135=
NM_001382802.1:c.3351T>G	NP_001369731.1:p.Ala1117=
NM_001382803.1:c.*188T>G	NP_001369732.1:n.*188T>G
NM_001382804.1:c.2781T>G	NP_001369733.1:p.Ala927=
NM_001382805.1:c.2658T>G	NP_001369734.1:p.Ala886=
NM_001382806.1:c.2571T>G	NP_001369735.1:p.Ala857=
NM_004448.4:c.3609T>G MANE Select	NP_004439.2:p.Ala1203=
NR_110535.2:n.3847T>G