Canonical Allele Identifier: CA499670878

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145849631
• MyVariant Identifiers: chr17:g.37881044A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724791A>T , CM000679.2:g.39724791A>T	GRCh38
NC_000017.10:g.37881044A>T , CM000679.1:g.37881044A>T	GRCh37
NC_000017.9:g.35134570A>T	NCBI36
NG_007503.1:g.41652A>T , LRG_724:g.41652A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2373A>T MANE Select	ENSP00000269571.4:p.Thr791=
ENST00000269571.9:c.2373A>T	ENSP00000269571.4:p.Thr791=
ENST00000406381.6:c.2283A>T	ENSP00000385185.2:p.Thr761=
ENST00000445658.6:c.1545A>T	ENSP00000404047.2:p.Thr515=
ENST00000541774.5:c.2328A>T	ENSP00000446466.1:p.Thr776=
ENST00000578373.5:c.*2163A>T	ENSP00000463427.1:n.*2163A>T
ENST00000580074.1:c.479A>T
ENST00000583038.5:n.3507A>T
ENST00000584450.5:c.2373A>T	ENSP00000463714.1:p.Thr791=
ENST00000584601.5:c.2283A>T	ENSP00000462438.1:p.Thr761=
NM_001005862.2:c.2283A>T , LRG_724t1:c.2283A>T	NP_001005862.1:p.Thr761=
NM_001289936.1:c.2328A>T , LRG_724t4:c.2328A>T	NP_001276865.1:p.Thr776=
NM_001289937.1:c.2373A>T	NP_001276866.1:p.Thr791=
NM_004448.3:c.2373A>T , LRG_724t2:c.2373A>T	NP_004439.2:p.Thr791=
NR_110535.1:n.2697A>T
XM_024450641.1:c.2511A>T	XP_024306409.1:p.Thr837=
XM_024450642.1:c.2466A>T	XP_024306410.1:p.Thr822=
XM_024450643.1:c.2421A>T	XP_024306411.1:p.Thr807=
NM_001005862.3:c.2283A>T	NP_001005862.1:p.Thr761=
NM_001289936.2:c.2328A>T	NP_001276865.1:p.Thr776=
NM_001289937.2:c.2373A>T	NP_001276866.1:p.Thr791=
NM_001382782.1:c.2283A>T	NP_001369711.1:p.Thr761=
NM_001382783.1:c.2283A>T	NP_001369712.1:p.Thr761=
NM_001382784.1:c.2490A>T	NP_001369713.1:p.Thr830=
NM_001382785.1:c.2475A>T	NP_001369714.1:p.Thr825=
NM_001382786.1:c.2454A>T	NP_001369715.1:p.Thr818=
NM_001382787.1:c.2448A>T	NP_001369716.1:p.Thr816=
NM_001382788.1:c.2403A>T	NP_001369717.1:p.Thr801=
NM_001382789.1:c.2394A>T	NP_001369718.1:p.Thr798=
NM_001382790.1:c.2370A>T	NP_001369719.1:p.Thr790=
NM_001382791.1:c.2364A>T	NP_001369720.1:p.Thr788=
NM_001382792.1:c.2337A>T	NP_001369721.1:p.Thr779=
NM_001382793.1:c.2331A>T	NP_001369722.1:p.Thr777=
NM_001382794.1:c.2331A>T	NP_001369723.1:p.Thr777=
NM_001382795.1:c.2325A>T	NP_001369724.1:p.Thr775=
NM_001382796.1:c.2373A>T	NP_001369725.1:p.Thr791=
NM_001382797.1:c.2274A>T	NP_001369726.1:p.Thr758=
NM_001382798.1:c.2373A>T	NP_001369727.1:p.Thr791=
NM_001382799.1:c.2193A>T	NP_001369728.1:p.Thr731=
NM_001382800.1:c.2308-258A>T	NP_001369729.1:n.2308-258A>T
NM_001382801.1:c.2325A>T	NP_001369730.1:p.Thr775=
NM_001382802.1:c.2115A>T	NP_001369731.1:p.Thr705=
NM_001382803.1:c.2331A>T	NP_001369732.1:p.Thr777=
NM_001382804.1:c.1545A>T	NP_001369733.1:p.Thr515=
NM_001382805.1:c.2208+1131A>T	NP_001369734.1:n.2208+1131A>T
NM_001382806.1:c.1335A>T	NP_001369735.1:p.Thr445=
NM_004448.4:c.2373A>T MANE Select	NP_004439.2:p.Thr791=
NR_110535.2:n.2611A>T