Canonical Allele Identifier: CA399304330

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145863443
• MyVariant Identifiers: chr17:g.37881337C>G (hg19) ; chr17:g.39725084C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725084C>G , CM000679.2:g.39725084C>G	GRCh38
NC_000017.10:g.37881337C>G , CM000679.1:g.37881337C>G	GRCh37
NC_000017.9:g.35134863C>G	NCBI36
NG_007503.1:g.41945C>G , LRG_724:g.41945C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2529C>G MANE Select	ENSP00000269571.4:p.His843Gln
ENST00000269571.9:c.2529C>G	ENSP00000269571.4:p.His843Gln
ENST00000406381.6:c.2439C>G	ENSP00000385185.2:p.His813Gln
ENST00000445658.6:c.1701C>G	ENSP00000404047.2:p.His567Gln
ENST00000541774.5:c.2484C>G	ENSP00000446466.1:p.His828Gln
ENST00000578373.5:c.*2319C>G	ENSP00000463427.1:n.*2319C>G
ENST00000580074.1:c.635C>G
ENST00000583038.5:n.3663C>G
ENST00000584450.5:c.2529C>G	ENSP00000463714.1:p.His843Gln
ENST00000584601.5:c.2439C>G	ENSP00000462438.1:p.His813Gln
NM_001005862.2:c.2439C>G , LRG_724t1:c.2439C>G	NP_001005862.1:p.His813Gln
NM_001289936.1:c.2484C>G , LRG_724t4:c.2484C>G	NP_001276865.1:p.His828Gln
NM_001289937.1:c.2529C>G	NP_001276866.1:p.His843Gln
NM_004448.3:c.2529C>G , LRG_724t2:c.2529C>G	NP_004439.2:p.His843Gln
NR_110535.1:n.2853C>G
XM_024450641.1:c.2667C>G	XP_024306409.1:p.His889Gln
XM_024450642.1:c.2622C>G	XP_024306410.1:p.His874Gln
XM_024450643.1:c.2577C>G	XP_024306411.1:p.His859Gln
NM_001005862.3:c.2439C>G	NP_001005862.1:p.His813Gln
NM_001289936.2:c.2484C>G	NP_001276865.1:p.His828Gln
NM_001289937.2:c.2529C>G	NP_001276866.1:p.His843Gln
NM_001382782.1:c.2439C>G	NP_001369711.1:p.His813Gln
NM_001382783.1:c.2439C>G	NP_001369712.1:p.His813Gln
NM_001382784.1:c.2646C>G	NP_001369713.1:p.His882Gln
NM_001382785.1:c.2631C>G	NP_001369714.1:p.His877Gln
NM_001382786.1:c.2610C>G	NP_001369715.1:p.His870Gln
NM_001382787.1:c.2604C>G	NP_001369716.1:p.His868Gln
NM_001382788.1:c.2559C>G	NP_001369717.1:p.His853Gln
NM_001382789.1:c.2550C>G	NP_001369718.1:p.His850Gln
NM_001382790.1:c.2526C>G	NP_001369719.1:p.His842Gln
NM_001382791.1:c.2520C>G	NP_001369720.1:p.His840Gln
NM_001382792.1:c.2493C>G	NP_001369721.1:p.His831Gln
NM_001382793.1:c.2487C>G	NP_001369722.1:p.His829Gln
NM_001382794.1:c.2487C>G	NP_001369723.1:p.His829Gln
NM_001382795.1:c.2481C>G	NP_001369724.1:p.His827Gln
NM_001382796.1:c.2529C>G	NP_001369725.1:p.His843Gln
NM_001382797.1:c.2430C>G	NP_001369726.1:p.His810Gln
NM_001382798.1:c.2493+173C>G	NP_001369727.1:n.2493+173C>G
NM_001382799.1:c.2349C>G	NP_001369728.1:p.His783Gln
NM_001382800.1:c.2343C>G	NP_001369729.1:p.His781Gln
NM_001382801.1:c.2445+173C>G	NP_001369730.1:n.2445+173C>G
NM_001382802.1:c.2271C>G	NP_001369731.1:p.His757Gln
NM_001382803.1:c.2487C>G	NP_001369732.1:p.His829Gln
NM_001382804.1:c.1701C>G	NP_001369733.1:p.His567Gln
NM_001382805.1:c.2208+1424C>G	NP_001369734.1:n.2208+1424C>G
NM_001382806.1:c.1491C>G	NP_001369735.1:p.His497Gln
NM_004448.4:c.2529C>G MANE Select	NP_004439.2:p.His843Gln
NR_110535.2:n.2767C>G