Canonical Allele Identifier: CA499890820

Gene: ERBB2

Linked Data

• dbSNP Id: rs1288263593
• gnomAD v2: 17-37884153-C-T
• gnomAD v4: 17-39727900-C-T
• MyVariant Identifiers: chr17:g.37884153C>T (hg19) ; chr17:g.39727900C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727900C>T , CM000679.2:g.39727900C>T	GRCh38
NC_000017.10:g.37884153C>T , CM000679.1:g.37884153C>T	GRCh37
NC_000017.9:g.35137679C>T	NCBI36
NG_007503.1:g.44761C>T , LRG_724:g.44761C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3624C>T MANE Select	ENSP00000269571.4:p.His1208=
ENST00000269571.9:c.3624C>T	ENSP00000269571.4:p.His1208=
ENST00000406381.6:c.3534C>T	ENSP00000385185.2:p.His1178=
ENST00000445658.6:c.2796C>T	ENSP00000404047.2:p.His932=
ENST00000541774.5:c.3579C>T	ENSP00000446466.1:p.His1193=
ENST00000578373.5:c.*3414C>T	ENSP00000463427.1:n.*3414C>T
ENST00000584450.5:c.*203C>T	ENSP00000463714.1:n.*203C>T
ENST00000584601.5:c.3534C>T	ENSP00000462438.1:p.His1178=
NM_001005862.2:c.3534C>T , LRG_724t1:c.3534C>T	NP_001005862.1:p.His1178=
NM_001289936.1:c.3579C>T , LRG_724t4:c.3579C>T	NP_001276865.1:p.His1193=
NM_001289937.1:c.*203C>T	NP_001276866.1:n.*203C>T
NM_004448.3:c.3624C>T , LRG_724t2:c.3624C>T	NP_004439.2:p.His1208=
NR_110535.1:n.3948C>T
XM_024450641.1:c.3762C>T	XP_024306409.1:p.His1254=
XM_024450642.1:c.3717C>T	XP_024306410.1:p.His1239=
XM_024450643.1:c.3672C>T	XP_024306411.1:p.His1224=
NM_001005862.3:c.3534C>T	NP_001005862.1:p.His1178=
NM_001289936.2:c.3579C>T	NP_001276865.1:p.His1193=
NM_001289937.2:c.*203C>T	NP_001276866.1:n.*203C>T
NM_001382782.1:c.3534C>T	NP_001369711.1:p.His1178=
NM_001382783.1:c.3534C>T	NP_001369712.1:p.His1178=
NM_001382784.1:c.3741C>T	NP_001369713.1:p.His1247=
NM_001382785.1:c.3726C>T	NP_001369714.1:p.His1242=
NM_001382786.1:c.3705C>T	NP_001369715.1:p.His1235=
NM_001382787.1:c.3699C>T	NP_001369716.1:p.His1233=
NM_001382788.1:c.3654C>T	NP_001369717.1:p.His1218=
NM_001382789.1:c.3645C>T	NP_001369718.1:p.His1215=
NM_001382790.1:c.3621C>T	NP_001369719.1:p.His1207=
NM_001382791.1:c.3615C>T	NP_001369720.1:p.His1205=
NM_001382792.1:c.3588C>T	NP_001369721.1:p.His1196=
NM_001382793.1:c.3582C>T	NP_001369722.1:p.His1194=
NM_001382794.1:c.3582C>T	NP_001369723.1:p.His1194=
NM_001382795.1:c.3576C>T	NP_001369724.1:p.His1192=
NM_001382796.1:c.3537C>T	NP_001369725.1:p.His1179=
NM_001382797.1:c.3525C>T	NP_001369726.1:p.His1175=
NM_001382798.1:c.3468C>T	NP_001369727.1:p.His1156=
NM_001382799.1:c.3444C>T	NP_001369728.1:p.His1148=
NM_001382800.1:c.3438C>T	NP_001369729.1:p.His1146=
NM_001382801.1:c.3420C>T	NP_001369730.1:p.His1140=
NM_001382802.1:c.3366C>T	NP_001369731.1:p.His1122=
NM_001382803.1:c.*203C>T	NP_001369732.1:n.*203C>T
NM_001382804.1:c.2796C>T	NP_001369733.1:p.His932=
NM_001382805.1:c.2673C>T	NP_001369734.1:p.His891=
NM_001382806.1:c.2586C>T	NP_001369735.1:p.His862=
NM_004448.4:c.3624C>T MANE Select	NP_004439.2:p.His1208=
NR_110535.2:n.3862C>T