Canonical Allele Identifier: CA499671688

Gene: ERBB2

Linked Data

• dbSNP Id: rs1350776870
• MyVariant Identifiers: chr17:g.37884222G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727969G>T , CM000679.2:g.39727969G>T	GRCh38
NC_000017.10:g.37884222G>T , CM000679.1:g.37884222G>T	GRCh37
NC_000017.9:g.35137748G>T	NCBI36
NG_007503.1:g.44830G>T , LRG_724:g.44830G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3693G>T MANE Select	ENSP00000269571.4:p.Gly1231=
ENST00000269571.9:c.3693G>T	ENSP00000269571.4:p.Gly1231=
ENST00000406381.6:c.3603G>T	ENSP00000385185.2:p.Gly1201=
ENST00000445658.6:c.2865G>T	ENSP00000404047.2:p.Gly955=
ENST00000541774.5:c.3648G>T	ENSP00000446466.1:p.Gly1216=
ENST00000578373.5:c.*3483G>T	ENSP00000463427.1:n.*3483G>T
ENST00000584450.5:c.*272G>T	ENSP00000463714.1:n.*272G>T
ENST00000584601.5:c.3603G>T	ENSP00000462438.1:p.Gly1201=
NM_001005862.2:c.3603G>T , LRG_724t1:c.3603G>T	NP_001005862.1:p.Gly1201=
NM_001289936.1:c.3648G>T , LRG_724t4:c.3648G>T	NP_001276865.1:p.Gly1216=
NM_001289937.1:c.*272G>T	NP_001276866.1:n.*272G>T
NM_004448.3:c.3693G>T , LRG_724t2:c.3693G>T	NP_004439.2:p.Gly1231=
NR_110535.1:n.4017G>T
XM_024450641.1:c.3831G>T	XP_024306409.1:p.Gly1277=
XM_024450642.1:c.3786G>T	XP_024306410.1:p.Gly1262=
XM_024450643.1:c.3741G>T	XP_024306411.1:p.Gly1247=
NM_001005862.3:c.3603G>T	NP_001005862.1:p.Gly1201=
NM_001289936.2:c.3648G>T	NP_001276865.1:p.Gly1216=
NM_001289937.2:c.*272G>T	NP_001276866.1:n.*272G>T
NM_001382782.1:c.3603G>T	NP_001369711.1:p.Gly1201=
NM_001382783.1:c.3603G>T	NP_001369712.1:p.Gly1201=
NM_001382784.1:c.3810G>T	NP_001369713.1:p.Gly1270=
NM_001382785.1:c.3795G>T	NP_001369714.1:p.Gly1265=
NM_001382786.1:c.3774G>T	NP_001369715.1:p.Gly1258=
NM_001382787.1:c.3768G>T	NP_001369716.1:p.Gly1256=
NM_001382788.1:c.3723G>T	NP_001369717.1:p.Gly1241=
NM_001382789.1:c.3714G>T	NP_001369718.1:p.Gly1238=
NM_001382790.1:c.3690G>T	NP_001369719.1:p.Gly1230=
NM_001382791.1:c.3684G>T	NP_001369720.1:p.Gly1228=
NM_001382792.1:c.3657G>T	NP_001369721.1:p.Gly1219=
NM_001382793.1:c.3651G>T	NP_001369722.1:p.Gly1217=
NM_001382794.1:c.3651G>T	NP_001369723.1:p.Gly1217=
NM_001382795.1:c.3645G>T	NP_001369724.1:p.Gly1215=
NM_001382796.1:c.3606G>T	NP_001369725.1:p.Gly1202=
NM_001382797.1:c.3594G>T	NP_001369726.1:p.Gly1198=
NM_001382798.1:c.3537G>T	NP_001369727.1:p.Gly1179=
NM_001382799.1:c.3513G>T	NP_001369728.1:p.Gly1171=
NM_001382800.1:c.3507G>T	NP_001369729.1:p.Gly1169=
NM_001382801.1:c.3489G>T	NP_001369730.1:p.Gly1163=
NM_001382802.1:c.3435G>T	NP_001369731.1:p.Gly1145=
NM_001382803.1:c.*272G>T	NP_001369732.1:n.*272G>T
NM_001382804.1:c.2865G>T	NP_001369733.1:p.Gly955=
NM_001382805.1:c.2742G>T	NP_001369734.1:p.Gly914=
NM_001382806.1:c.2655G>T	NP_001369735.1:p.Gly885=
NM_004448.4:c.3693G>T MANE Select	NP_004439.2:p.Gly1231=
NR_110535.2:n.3931G>T