Canonical Allele Identifier: CA399303339
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs1238981206

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39724828G>C , CM000679.2:g.39724828G>C GRCh38
NC_000017.10:g.37881081G>C , CM000679.1:g.37881081G>C GRCh37
NC_000017.9:g.35134607G>C NCBI36
NG_007503.1:g.41689G>C , LRG_724:g.41689G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2410G>C MANE Select ENSP00000269571.4:p.Gly804Arg
ENST00000269571.9:c.2410G>C ENSP00000269571.4:p.Gly804Arg
ENST00000406381.6:c.2320G>C ENSP00000385185.2:p.Gly774Arg
ENST00000445658.6:c.1582G>C ENSP00000404047.2:p.Gly528Arg
ENST00000541774.5:c.2365G>C ENSP00000446466.1:p.Gly789Arg
ENST00000578373.5:c.*2200G>C ENSP00000463427.1:n.*2200G>C
ENST00000580074.1:c.516G>C
ENST00000583038.5:n.3544G>C
ENST00000584450.5:c.2410G>C ENSP00000463714.1:p.Gly804Arg
ENST00000584601.5:c.2320G>C ENSP00000462438.1:p.Gly774Arg
NM_001005862.2:c.2320G>C , LRG_724t1:c.2320G>C NP_001005862.1:p.Gly774Arg
NM_001289936.1:c.2365G>C , LRG_724t4:c.2365G>C NP_001276865.1:p.Gly789Arg
NM_001289937.1:c.2410G>C NP_001276866.1:p.Gly804Arg
NM_004448.3:c.2410G>C , LRG_724t2:c.2410G>C NP_004439.2:p.Gly804Arg
NR_110535.1:n.2734G>C
XM_024450641.1:c.2548G>C XP_024306409.1:p.Gly850Arg
XM_024450642.1:c.2503G>C XP_024306410.1:p.Gly835Arg
XM_024450643.1:c.2458G>C XP_024306411.1:p.Gly820Arg
NM_001005862.3:c.2320G>C NP_001005862.1:p.Gly774Arg
NM_001289936.2:c.2365G>C NP_001276865.1:p.Gly789Arg
NM_001289937.2:c.2410G>C NP_001276866.1:p.Gly804Arg
NM_001382782.1:c.2320G>C NP_001369711.1:p.Gly774Arg
NM_001382783.1:c.2320G>C NP_001369712.1:p.Gly774Arg
NM_001382784.1:c.2527G>C NP_001369713.1:p.Gly843Arg
NM_001382785.1:c.2512G>C NP_001369714.1:p.Gly838Arg
NM_001382786.1:c.2491G>C NP_001369715.1:p.Gly831Arg
NM_001382787.1:c.2485G>C NP_001369716.1:p.Gly829Arg
NM_001382788.1:c.2440G>C NP_001369717.1:p.Gly814Arg
NM_001382789.1:c.2431G>C NP_001369718.1:p.Gly811Arg
NM_001382790.1:c.2407G>C NP_001369719.1:p.Gly803Arg
NM_001382791.1:c.2401G>C NP_001369720.1:p.Gly801Arg
NM_001382792.1:c.2374G>C NP_001369721.1:p.Gly792Arg
NM_001382793.1:c.2368G>C NP_001369722.1:p.Gly790Arg
NM_001382794.1:c.2368G>C NP_001369723.1:p.Gly790Arg
NM_001382795.1:c.2362G>C NP_001369724.1:p.Gly788Arg
NM_001382796.1:c.2410G>C NP_001369725.1:p.Gly804Arg
NM_001382797.1:c.2311G>C NP_001369726.1:p.Gly771Arg
NM_001382798.1:c.2410G>C NP_001369727.1:p.Gly804Arg
NM_001382799.1:c.2230G>C NP_001369728.1:p.Gly744Arg
NM_001382800.1:c.2308-221G>C NP_001369729.1:n.2308-221G>C
NM_001382801.1:c.2362G>C NP_001369730.1:p.Gly788Arg
NM_001382802.1:c.2152G>C NP_001369731.1:p.Gly718Arg
NM_001382803.1:c.2368G>C NP_001369732.1:p.Gly790Arg
NM_001382804.1:c.1582G>C NP_001369733.1:p.Gly528Arg
NM_001382805.1:c.2208+1168G>C NP_001369734.1:n.2208+1168G>C
NM_001382806.1:c.1372G>C NP_001369735.1:p.Gly458Arg
NM_004448.4:c.2410G>C MANE Select NP_004439.2:p.Gly804Arg
NR_110535.2:n.2648G>C