Canonical Allele Identifier: CA399304424
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2145864111

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39725100C>G , CM000679.2:g.39725100C>G GRCh38
NC_000017.10:g.37881353C>G , CM000679.1:g.37881353C>G GRCh37
NC_000017.9:g.35134879C>G NCBI36
NG_007503.1:g.41961C>G , LRG_724:g.41961C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2545C>G MANE Select ENSP00000269571.4:p.Arg849Gly
ENST00000269571.9:c.2545C>G ENSP00000269571.4:p.Arg849Gly
ENST00000406381.6:c.2455C>G ENSP00000385185.2:p.Arg819Gly
ENST00000445658.6:c.1717C>G ENSP00000404047.2:p.Arg573Gly
ENST00000541774.5:c.2500C>G ENSP00000446466.1:p.Arg834Gly
ENST00000578373.5:c.*2335C>G ENSP00000463427.1:n.*2335C>G
ENST00000580074.1:c.651C>G
ENST00000583038.5:n.3679C>G
ENST00000584450.5:c.2545C>G ENSP00000463714.1:p.Arg849Gly
ENST00000584601.5:c.2455C>G ENSP00000462438.1:p.Arg819Gly
NM_001005862.2:c.2455C>G , LRG_724t1:c.2455C>G NP_001005862.1:p.Arg819Gly
NM_001289936.1:c.2500C>G , LRG_724t4:c.2500C>G NP_001276865.1:p.Arg834Gly
NM_001289937.1:c.2545C>G NP_001276866.1:p.Arg849Gly
NM_004448.3:c.2545C>G , LRG_724t2:c.2545C>G NP_004439.2:p.Arg849Gly
NR_110535.1:n.2869C>G
XM_024450641.1:c.2683C>G XP_024306409.1:p.Arg895Gly
XM_024450642.1:c.2638C>G XP_024306410.1:p.Arg880Gly
XM_024450643.1:c.2593C>G XP_024306411.1:p.Arg865Gly
NM_001005862.3:c.2455C>G NP_001005862.1:p.Arg819Gly
NM_001289936.2:c.2500C>G NP_001276865.1:p.Arg834Gly
NM_001289937.2:c.2545C>G NP_001276866.1:p.Arg849Gly
NM_001382782.1:c.2455C>G NP_001369711.1:p.Arg819Gly
NM_001382783.1:c.2455C>G NP_001369712.1:p.Arg819Gly
NM_001382784.1:c.2662C>G NP_001369713.1:p.Arg888Gly
NM_001382785.1:c.2647C>G NP_001369714.1:p.Arg883Gly
NM_001382786.1:c.2626C>G NP_001369715.1:p.Arg876Gly
NM_001382787.1:c.2620C>G NP_001369716.1:p.Arg874Gly
NM_001382788.1:c.2575C>G NP_001369717.1:p.Arg859Gly
NM_001382789.1:c.2566C>G NP_001369718.1:p.Arg856Gly
NM_001382790.1:c.2542C>G NP_001369719.1:p.Arg848Gly
NM_001382791.1:c.2536C>G NP_001369720.1:p.Arg846Gly
NM_001382792.1:c.2509C>G NP_001369721.1:p.Arg837Gly
NM_001382793.1:c.2503C>G NP_001369722.1:p.Arg835Gly
NM_001382794.1:c.2503C>G NP_001369723.1:p.Arg835Gly
NM_001382795.1:c.2497C>G NP_001369724.1:p.Arg833Gly
NM_001382796.1:c.2545C>G NP_001369725.1:p.Arg849Gly
NM_001382797.1:c.2446C>G NP_001369726.1:p.Arg816Gly
NM_001382798.1:c.2493+189C>G NP_001369727.1:n.2493+189C>G
NM_001382799.1:c.2365C>G NP_001369728.1:p.Arg789Gly
NM_001382800.1:c.2359C>G NP_001369729.1:p.Arg787Gly
NM_001382801.1:c.2445+189C>G NP_001369730.1:n.2445+189C>G
NM_001382802.1:c.2287C>G NP_001369731.1:p.Arg763Gly
NM_001382803.1:c.2503C>G NP_001369732.1:p.Arg835Gly
NM_001382804.1:c.1717C>G NP_001369733.1:p.Arg573Gly
NM_001382805.1:c.2208+1440C>G NP_001369734.1:n.2208+1440C>G
NM_001382806.1:c.1507C>G NP_001369735.1:p.Arg503Gly
NM_004448.4:c.2545C>G MANE Select NP_004439.2:p.Arg849Gly
NR_110535.2:n.2783C>G