Canonical Allele Identifier: CA499670840

Gene: ERBB2

Linked Data

• dbSNP Id: rs1597886487
• MyVariant Identifiers: chr17:g.37880999T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724746T>G , CM000679.2:g.39724746T>G	GRCh38
NC_000017.10:g.37880999T>G , CM000679.1:g.37880999T>G	GRCh37
NC_000017.9:g.35134525T>G	NCBI36
NG_007503.1:g.41607T>G , LRG_724:g.41607T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2328T>G MANE Select	ENSP00000269571.4:p.Gly776=
ENST00000269571.9:c.2328T>G	ENSP00000269571.4:p.Gly776=
ENST00000406381.6:c.2238T>G	ENSP00000385185.2:p.Gly746=
ENST00000445658.6:c.1500T>G	ENSP00000404047.2:p.Gly500=
ENST00000541774.5:c.2283T>G	ENSP00000446466.1:p.Gly761=
ENST00000578373.5:c.*2118T>G	ENSP00000463427.1:n.*2118T>G
ENST00000580074.1:c.434T>G
ENST00000583038.5:n.3462T>G
ENST00000584450.5:c.2328T>G	ENSP00000463714.1:p.Gly776=
ENST00000584601.5:c.2238T>G	ENSP00000462438.1:p.Gly746=
NM_001005862.2:c.2238T>G , LRG_724t1:c.2238T>G	NP_001005862.1:p.Gly746=
NM_001289936.1:c.2283T>G , LRG_724t4:c.2283T>G	NP_001276865.1:p.Gly761=
NM_001289937.1:c.2328T>G	NP_001276866.1:p.Gly776=
NM_004448.3:c.2328T>G , LRG_724t2:c.2328T>G	NP_004439.2:p.Gly776=
NR_110535.1:n.2652T>G
XM_024450641.1:c.2466T>G	XP_024306409.1:p.Gly822=
XM_024450642.1:c.2421T>G	XP_024306410.1:p.Gly807=
XM_024450643.1:c.2376T>G	XP_024306411.1:p.Gly792=
NM_001005862.3:c.2238T>G	NP_001005862.1:p.Gly746=
NM_001289936.2:c.2283T>G	NP_001276865.1:p.Gly761=
NM_001289937.2:c.2328T>G	NP_001276866.1:p.Gly776=
NM_001382782.1:c.2238T>G	NP_001369711.1:p.Gly746=
NM_001382783.1:c.2238T>G	NP_001369712.1:p.Gly746=
NM_001382784.1:c.2445T>G	NP_001369713.1:p.Gly815=
NM_001382785.1:c.2430T>G	NP_001369714.1:p.Gly810=
NM_001382786.1:c.2409T>G	NP_001369715.1:p.Gly803=
NM_001382787.1:c.2403T>G	NP_001369716.1:p.Gly801=
NM_001382788.1:c.2358T>G	NP_001369717.1:p.Gly786=
NM_001382789.1:c.2349T>G	NP_001369718.1:p.Gly783=
NM_001382790.1:c.2325T>G	NP_001369719.1:p.Gly775=
NM_001382791.1:c.2319T>G	NP_001369720.1:p.Gly773=
NM_001382792.1:c.2292T>G	NP_001369721.1:p.Gly764=
NM_001382793.1:c.2286T>G	NP_001369722.1:p.Gly762=
NM_001382794.1:c.2286T>G	NP_001369723.1:p.Gly762=
NM_001382795.1:c.2280T>G	NP_001369724.1:p.Gly760=
NM_001382796.1:c.2328T>G	NP_001369725.1:p.Gly776=
NM_001382797.1:c.2229T>G	NP_001369726.1:p.Gly743=
NM_001382798.1:c.2328T>G	NP_001369727.1:p.Gly776=
NM_001382799.1:c.2148T>G	NP_001369728.1:p.Gly716=
NM_001382800.1:c.2308-303T>G	NP_001369729.1:n.2308-303T>G
NM_001382801.1:c.2280T>G	NP_001369730.1:p.Gly760=
NM_001382802.1:c.2070T>G	NP_001369731.1:p.Gly690=
NM_001382803.1:c.2286T>G	NP_001369732.1:p.Gly762=
NM_001382804.1:c.1500T>G	NP_001369733.1:p.Gly500=
NM_001382805.1:c.2208+1086T>G	NP_001369734.1:n.2208+1086T>G
NM_001382806.1:c.1290T>G	NP_001369735.1:p.Gly430=
NM_004448.4:c.2328T>G MANE Select	NP_004439.2:p.Gly776=
NR_110535.2:n.2566T>G