Canonical Allele Identifier: CA399304647

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145865223
• MyVariant Identifiers: chr17:g.37881380C>T (hg19) ; chr17:g.39725127C>T (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2572C>T MANE Select	ENSP00000269571.4:p.His858Tyr
ENST00000269571.9:c.2572C>T	ENSP00000269571.4:p.His858Tyr
ENST00000406381.6:c.2482C>T	ENSP00000385185.2:p.His828Tyr
ENST00000445658.6:c.1744C>T	ENSP00000404047.2:p.His582Tyr
ENST00000541774.5:c.2527C>T	ENSP00000446466.1:p.His843Tyr
ENST00000578373.5:c.*2362C>T	ENSP00000463427.1:n.*2362C>T
ENST00000580074.1:c.678C>T
ENST00000583038.5:n.3706C>T
ENST00000584450.5:c.2572C>T	ENSP00000463714.1:p.His858Tyr
ENST00000584601.5:c.2482C>T	ENSP00000462438.1:p.His828Tyr
NM_001005862.2:c.2482C>T , LRG_724t1:c.2482C>T	NP_001005862.1:p.His828Tyr
NM_001289936.1:c.2527C>T , LRG_724t4:c.2527C>T	NP_001276865.1:p.His843Tyr
NM_001289937.1:c.2572C>T	NP_001276866.1:p.His858Tyr
NM_004448.3:c.2572C>T , LRG_724t2:c.2572C>T	NP_004439.2:p.His858Tyr
NR_110535.1:n.2896C>T
XM_024450641.1:c.2710C>T	XP_024306409.1:p.His904Tyr
XM_024450642.1:c.2665C>T	XP_024306410.1:p.His889Tyr
XM_024450643.1:c.2620C>T	XP_024306411.1:p.His874Tyr
NM_001005862.3:c.2482C>T	NP_001005862.1:p.His828Tyr
NM_001289936.2:c.2527C>T	NP_001276865.1:p.His843Tyr
NM_001289937.2:c.2572C>T	NP_001276866.1:p.His858Tyr
NM_001382782.1:c.2482C>T	NP_001369711.1:p.His828Tyr
NM_001382783.1:c.2482C>T	NP_001369712.1:p.His828Tyr
NM_001382784.1:c.2689C>T	NP_001369713.1:p.His897Tyr
NM_001382785.1:c.2674C>T	NP_001369714.1:p.His892Tyr
NM_001382786.1:c.2653C>T	NP_001369715.1:p.His885Tyr
NM_001382787.1:c.2647C>T	NP_001369716.1:p.His883Tyr
NM_001382788.1:c.2602C>T	NP_001369717.1:p.His868Tyr
NM_001382789.1:c.2593C>T	NP_001369718.1:p.His865Tyr
NM_001382790.1:c.2569C>T	NP_001369719.1:p.His857Tyr
NM_001382791.1:c.2563C>T	NP_001369720.1:p.His855Tyr
NM_001382792.1:c.2536C>T	NP_001369721.1:p.His846Tyr
NM_001382793.1:c.2530C>T	NP_001369722.1:p.His844Tyr
NM_001382794.1:c.2530C>T	NP_001369723.1:p.His844Tyr
NM_001382795.1:c.2524C>T	NP_001369724.1:p.His842Tyr
NM_001382796.1:c.2572C>T	NP_001369725.1:p.His858Tyr
NM_001382797.1:c.2473C>T	NP_001369726.1:p.His825Tyr
NM_001382798.1:c.2494-200C>T	NP_001369727.1:n.2494-200C>T
NM_001382799.1:c.2392C>T	NP_001369728.1:p.His798Tyr
NM_001382800.1:c.2386C>T	NP_001369729.1:p.His796Tyr
NM_001382801.1:c.2446-200C>T	NP_001369730.1:n.2446-200C>T
NM_001382802.1:c.2314C>T	NP_001369731.1:p.His772Tyr
NM_001382803.1:c.2530C>T	NP_001369732.1:p.His844Tyr
NM_001382804.1:c.1744C>T	NP_001369733.1:p.His582Tyr
NM_001382805.1:c.2208+1467C>T	NP_001369734.1:n.2208+1467C>T
NM_001382806.1:c.1534C>T	NP_001369735.1:p.His512Tyr
NM_004448.4:c.2572C>T MANE Select	NP_004439.2:p.His858Tyr
NR_110535.2:n.2810C>T