Canonical Allele Identifier: CA399304296
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2145863361

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39725082C>G , CM000679.2:g.39725082C>G GRCh38
NC_000017.10:g.37881335C>G , CM000679.1:g.37881335C>G GRCh37
NC_000017.9:g.35134861C>G NCBI36
NG_007503.1:g.41943C>G , LRG_724:g.41943C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000269571.10:c.2527C>G MANE Select ENSP00000269571.4:p.His843Asp
ENST00000269571.9:c.2527C>G ENSP00000269571.4:p.His843Asp
ENST00000406381.6:c.2437C>G ENSP00000385185.2:p.His813Asp
ENST00000445658.6:c.1699C>G ENSP00000404047.2:p.His567Asp
ENST00000541774.5:c.2482C>G ENSP00000446466.1:p.His828Asp
ENST00000578373.5:c.*2317C>G ENSP00000463427.1:n.*2317C>G
ENST00000580074.1:c.633C>G
ENST00000583038.5:n.3661C>G
ENST00000584450.5:c.2527C>G ENSP00000463714.1:p.His843Asp
ENST00000584601.5:c.2437C>G ENSP00000462438.1:p.His813Asp
NM_001005862.2:c.2437C>G , LRG_724t1:c.2437C>G NP_001005862.1:p.His813Asp
NM_001289936.1:c.2482C>G , LRG_724t4:c.2482C>G NP_001276865.1:p.His828Asp
NM_001289937.1:c.2527C>G NP_001276866.1:p.His843Asp
NM_004448.3:c.2527C>G , LRG_724t2:c.2527C>G NP_004439.2:p.His843Asp
NR_110535.1:n.2851C>G
XM_024450641.1:c.2665C>G XP_024306409.1:p.His889Asp
XM_024450642.1:c.2620C>G XP_024306410.1:p.His874Asp
XM_024450643.1:c.2575C>G XP_024306411.1:p.His859Asp
NM_001005862.3:c.2437C>G NP_001005862.1:p.His813Asp
NM_001289936.2:c.2482C>G NP_001276865.1:p.His828Asp
NM_001289937.2:c.2527C>G NP_001276866.1:p.His843Asp
NM_001382782.1:c.2437C>G NP_001369711.1:p.His813Asp
NM_001382783.1:c.2437C>G NP_001369712.1:p.His813Asp
NM_001382784.1:c.2644C>G NP_001369713.1:p.His882Asp
NM_001382785.1:c.2629C>G NP_001369714.1:p.His877Asp
NM_001382786.1:c.2608C>G NP_001369715.1:p.His870Asp
NM_001382787.1:c.2602C>G NP_001369716.1:p.His868Asp
NM_001382788.1:c.2557C>G NP_001369717.1:p.His853Asp
NM_001382789.1:c.2548C>G NP_001369718.1:p.His850Asp
NM_001382790.1:c.2524C>G NP_001369719.1:p.His842Asp
NM_001382791.1:c.2518C>G NP_001369720.1:p.His840Asp
NM_001382792.1:c.2491C>G NP_001369721.1:p.His831Asp
NM_001382793.1:c.2485C>G NP_001369722.1:p.His829Asp
NM_001382794.1:c.2485C>G NP_001369723.1:p.His829Asp
NM_001382795.1:c.2479C>G NP_001369724.1:p.His827Asp
NM_001382796.1:c.2527C>G NP_001369725.1:p.His843Asp
NM_001382797.1:c.2428C>G NP_001369726.1:p.His810Asp
NM_001382798.1:c.2493+171C>G NP_001369727.1:n.2493+171C>G
NM_001382799.1:c.2347C>G NP_001369728.1:p.His783Asp
NM_001382800.1:c.2341C>G NP_001369729.1:p.His781Asp
NM_001382801.1:c.2445+171C>G NP_001369730.1:n.2445+171C>G
NM_001382802.1:c.2269C>G NP_001369731.1:p.His757Asp
NM_001382803.1:c.2485C>G NP_001369732.1:p.His829Asp
NM_001382804.1:c.1699C>G NP_001369733.1:p.His567Asp
NM_001382805.1:c.2208+1422C>G NP_001369734.1:n.2208+1422C>G
NM_001382806.1:c.1489C>G NP_001369735.1:p.His497Asp
NM_004448.4:c.2527C>G MANE Select NP_004439.2:p.His843Asp
NR_110535.2:n.2765C>G