Canonical Allele Identifier: CA499890092

Gene: ERBB2

Linked Data

• dbSNP Id: rs104886011
• MyVariant Identifiers: chr17:g.37881328G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725075G>C , CM000679.2:g.39725075G>C	GRCh38
NC_000017.10:g.37881328G>C , CM000679.1:g.37881328G>C	GRCh37
NC_000017.9:g.35134854G>C	NCBI36
NG_007503.1:g.41936G>C , LRG_724:g.41936G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2520G>C MANE Select	ENSP00000269571.4:p.Arg840=
ENST00000269571.9:c.2520G>C	ENSP00000269571.4:p.Arg840=
ENST00000406381.6:c.2430G>C	ENSP00000385185.2:p.Arg810=
ENST00000445658.6:c.1692G>C	ENSP00000404047.2:p.Arg564=
ENST00000541774.5:c.2475G>C	ENSP00000446466.1:p.Arg825=
ENST00000578373.5:c.*2310G>C	ENSP00000463427.1:n.*2310G>C
ENST00000580074.1:c.626G>C
ENST00000583038.5:n.3654G>C
ENST00000584450.5:c.2520G>C	ENSP00000463714.1:p.Arg840=
ENST00000584601.5:c.2430G>C	ENSP00000462438.1:p.Arg810=
NM_001005862.2:c.2430G>C , LRG_724t1:c.2430G>C	NP_001005862.1:p.Arg810=
NM_001289936.1:c.2475G>C , LRG_724t4:c.2475G>C	NP_001276865.1:p.Arg825=
NM_001289937.1:c.2520G>C	NP_001276866.1:p.Arg840=
NM_004448.3:c.2520G>C , LRG_724t2:c.2520G>C	NP_004439.2:p.Arg840=
NR_110535.1:n.2844G>C
XM_024450641.1:c.2658G>C	XP_024306409.1:p.Arg886=
XM_024450642.1:c.2613G>C	XP_024306410.1:p.Arg871=
XM_024450643.1:c.2568G>C	XP_024306411.1:p.Arg856=
NM_001005862.3:c.2430G>C	NP_001005862.1:p.Arg810=
NM_001289936.2:c.2475G>C	NP_001276865.1:p.Arg825=
NM_001289937.2:c.2520G>C	NP_001276866.1:p.Arg840=
NM_001382782.1:c.2430G>C	NP_001369711.1:p.Arg810=
NM_001382783.1:c.2430G>C	NP_001369712.1:p.Arg810=
NM_001382784.1:c.2637G>C	NP_001369713.1:p.Arg879=
NM_001382785.1:c.2622G>C	NP_001369714.1:p.Arg874=
NM_001382786.1:c.2601G>C	NP_001369715.1:p.Arg867=
NM_001382787.1:c.2595G>C	NP_001369716.1:p.Arg865=
NM_001382788.1:c.2550G>C	NP_001369717.1:p.Arg850=
NM_001382789.1:c.2541G>C	NP_001369718.1:p.Arg847=
NM_001382790.1:c.2517G>C	NP_001369719.1:p.Arg839=
NM_001382791.1:c.2511G>C	NP_001369720.1:p.Arg837=
NM_001382792.1:c.2484G>C	NP_001369721.1:p.Arg828=
NM_001382793.1:c.2478G>C	NP_001369722.1:p.Arg826=
NM_001382794.1:c.2478G>C	NP_001369723.1:p.Arg826=
NM_001382795.1:c.2472G>C	NP_001369724.1:p.Arg824=
NM_001382796.1:c.2520G>C	NP_001369725.1:p.Arg840=
NM_001382797.1:c.2421G>C	NP_001369726.1:p.Arg807=
NM_001382798.1:c.2493+164G>C	NP_001369727.1:n.2493+164G>C
NM_001382799.1:c.2340G>C	NP_001369728.1:p.Arg780=
NM_001382800.1:c.2334G>C	NP_001369729.1:p.Arg778=
NM_001382801.1:c.2445+164G>C	NP_001369730.1:n.2445+164G>C
NM_001382802.1:c.2262G>C	NP_001369731.1:p.Arg754=
NM_001382803.1:c.2478G>C	NP_001369732.1:p.Arg826=
NM_001382804.1:c.1692G>C	NP_001369733.1:p.Arg564=
NM_001382805.1:c.2208+1415G>C	NP_001369734.1:n.2208+1415G>C
NM_001382806.1:c.1482G>C	NP_001369735.1:p.Arg494=
NM_004448.4:c.2520G>C MANE Select	NP_004439.2:p.Arg840=
NR_110535.2:n.2758G>C