Canonical Allele Identifier: CA399304644
Gene: ERBB2 HGNC NCBI

Linked Data

dbSNP Id: rs2145865223

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39725127C>G , CM000679.2:g.39725127C>G GRCh38
NC_000017.10:g.37881380C>G , CM000679.1:g.37881380C>G GRCh37
NC_000017.9:g.35134906C>G NCBI36
NG_007503.1:g.41988C>G , LRG_724:g.41988C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000269571.10:c.2572C>G MANE Select ENSP00000269571.4:p.His858Asp
ENST00000269571.9:c.2572C>G ENSP00000269571.4:p.His858Asp
ENST00000406381.6:c.2482C>G ENSP00000385185.2:p.His828Asp
ENST00000445658.6:c.1744C>G ENSP00000404047.2:p.His582Asp
ENST00000541774.5:c.2527C>G ENSP00000446466.1:p.His843Asp
ENST00000578373.5:c.*2362C>G ENSP00000463427.1:n.*2362C>G
ENST00000580074.1:c.678C>G
ENST00000583038.5:n.3706C>G
ENST00000584450.5:c.2572C>G ENSP00000463714.1:p.His858Asp
ENST00000584601.5:c.2482C>G ENSP00000462438.1:p.His828Asp
NM_001005862.2:c.2482C>G , LRG_724t1:c.2482C>G NP_001005862.1:p.His828Asp
NM_001289936.1:c.2527C>G , LRG_724t4:c.2527C>G NP_001276865.1:p.His843Asp
NM_001289937.1:c.2572C>G NP_001276866.1:p.His858Asp
NM_004448.3:c.2572C>G , LRG_724t2:c.2572C>G NP_004439.2:p.His858Asp
NR_110535.1:n.2896C>G
XM_024450641.1:c.2710C>G XP_024306409.1:p.His904Asp
XM_024450642.1:c.2665C>G XP_024306410.1:p.His889Asp
XM_024450643.1:c.2620C>G XP_024306411.1:p.His874Asp
NM_001005862.3:c.2482C>G NP_001005862.1:p.His828Asp
NM_001289936.2:c.2527C>G NP_001276865.1:p.His843Asp
NM_001289937.2:c.2572C>G NP_001276866.1:p.His858Asp
NM_001382782.1:c.2482C>G NP_001369711.1:p.His828Asp
NM_001382783.1:c.2482C>G NP_001369712.1:p.His828Asp
NM_001382784.1:c.2689C>G NP_001369713.1:p.His897Asp
NM_001382785.1:c.2674C>G NP_001369714.1:p.His892Asp
NM_001382786.1:c.2653C>G NP_001369715.1:p.His885Asp
NM_001382787.1:c.2647C>G NP_001369716.1:p.His883Asp
NM_001382788.1:c.2602C>G NP_001369717.1:p.His868Asp
NM_001382789.1:c.2593C>G NP_001369718.1:p.His865Asp
NM_001382790.1:c.2569C>G NP_001369719.1:p.His857Asp
NM_001382791.1:c.2563C>G NP_001369720.1:p.His855Asp
NM_001382792.1:c.2536C>G NP_001369721.1:p.His846Asp
NM_001382793.1:c.2530C>G NP_001369722.1:p.His844Asp
NM_001382794.1:c.2530C>G NP_001369723.1:p.His844Asp
NM_001382795.1:c.2524C>G NP_001369724.1:p.His842Asp
NM_001382796.1:c.2572C>G NP_001369725.1:p.His858Asp
NM_001382797.1:c.2473C>G NP_001369726.1:p.His825Asp
NM_001382798.1:c.2494-200C>G NP_001369727.1:n.2494-200C>G
NM_001382799.1:c.2392C>G NP_001369728.1:p.His798Asp
NM_001382800.1:c.2386C>G NP_001369729.1:p.His796Asp
NM_001382801.1:c.2446-200C>G NP_001369730.1:n.2446-200C>G
NM_001382802.1:c.2314C>G NP_001369731.1:p.His772Asp
NM_001382803.1:c.2530C>G NP_001369732.1:p.His844Asp
NM_001382804.1:c.1744C>G NP_001369733.1:p.His582Asp
NM_001382805.1:c.2208+1467C>G NP_001369734.1:n.2208+1467C>G
NM_001382806.1:c.1534C>G NP_001369735.1:p.His512Asp
NM_004448.4:c.2572C>G MANE Select NP_004439.2:p.His858Asp
NR_110535.2:n.2810C>G