Canonical Allele Identifier: CA499670857

Gene: ERBB2

Linked Data

• dbSNP Id: rs763795273
• MyVariant Identifiers: chr17:g.37881020C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724767C>G , CM000679.2:g.39724767C>G	GRCh38
NC_000017.10:g.37881020C>G , CM000679.1:g.37881020C>G	GRCh37
NC_000017.9:g.35134546C>G	NCBI36
NG_007503.1:g.41628C>G , LRG_724:g.41628C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2349C>G MANE Select	ENSP00000269571.4:p.Ser783=
ENST00000269571.9:c.2349C>G	ENSP00000269571.4:p.Ser783=
ENST00000406381.6:c.2259C>G	ENSP00000385185.2:p.Ser753=
ENST00000445658.6:c.1521C>G	ENSP00000404047.2:p.Ser507=
ENST00000541774.5:c.2304C>G	ENSP00000446466.1:p.Ser768=
ENST00000578373.5:c.*2139C>G	ENSP00000463427.1:n.*2139C>G
ENST00000580074.1:c.455C>G
ENST00000583038.5:n.3483C>G
ENST00000584450.5:c.2349C>G	ENSP00000463714.1:p.Ser783=
ENST00000584601.5:c.2259C>G	ENSP00000462438.1:p.Ser753=
NM_001005862.2:c.2259C>G , LRG_724t1:c.2259C>G	NP_001005862.1:p.Ser753=
NM_001289936.1:c.2304C>G , LRG_724t4:c.2304C>G	NP_001276865.1:p.Ser768=
NM_001289937.1:c.2349C>G	NP_001276866.1:p.Ser783=
NM_004448.3:c.2349C>G , LRG_724t2:c.2349C>G	NP_004439.2:p.Ser783=
NR_110535.1:n.2673C>G
XM_024450641.1:c.2487C>G	XP_024306409.1:p.Ser829=
XM_024450642.1:c.2442C>G	XP_024306410.1:p.Ser814=
XM_024450643.1:c.2397C>G	XP_024306411.1:p.Ser799=
NM_001005862.3:c.2259C>G	NP_001005862.1:p.Ser753=
NM_001289936.2:c.2304C>G	NP_001276865.1:p.Ser768=
NM_001289937.2:c.2349C>G	NP_001276866.1:p.Ser783=
NM_001382782.1:c.2259C>G	NP_001369711.1:p.Ser753=
NM_001382783.1:c.2259C>G	NP_001369712.1:p.Ser753=
NM_001382784.1:c.2466C>G	NP_001369713.1:p.Ser822=
NM_001382785.1:c.2451C>G	NP_001369714.1:p.Ser817=
NM_001382786.1:c.2430C>G	NP_001369715.1:p.Ser810=
NM_001382787.1:c.2424C>G	NP_001369716.1:p.Ser808=
NM_001382788.1:c.2379C>G	NP_001369717.1:p.Ser793=
NM_001382789.1:c.2370C>G	NP_001369718.1:p.Ser790=
NM_001382790.1:c.2346C>G	NP_001369719.1:p.Ser782=
NM_001382791.1:c.2340C>G	NP_001369720.1:p.Ser780=
NM_001382792.1:c.2313C>G	NP_001369721.1:p.Ser771=
NM_001382793.1:c.2307C>G	NP_001369722.1:p.Ser769=
NM_001382794.1:c.2307C>G	NP_001369723.1:p.Ser769=
NM_001382795.1:c.2301C>G	NP_001369724.1:p.Ser767=
NM_001382796.1:c.2349C>G	NP_001369725.1:p.Ser783=
NM_001382797.1:c.2250C>G	NP_001369726.1:p.Ser750=
NM_001382798.1:c.2349C>G	NP_001369727.1:p.Ser783=
NM_001382799.1:c.2169C>G	NP_001369728.1:p.Ser723=
NM_001382800.1:c.2308-282C>G	NP_001369729.1:n.2308-282C>G
NM_001382801.1:c.2301C>G	NP_001369730.1:p.Ser767=
NM_001382802.1:c.2091C>G	NP_001369731.1:p.Ser697=
NM_001382803.1:c.2307C>G	NP_001369732.1:p.Ser769=
NM_001382804.1:c.1521C>G	NP_001369733.1:p.Ser507=
NM_001382805.1:c.2208+1107C>G	NP_001369734.1:n.2208+1107C>G
NM_001382806.1:c.1311C>G	NP_001369735.1:p.Ser437=
NM_004448.4:c.2349C>G MANE Select	NP_004439.2:p.Ser783=
NR_110535.2:n.2587C>G