Canonical Allele Identifier: CA499670884

Gene: ERBB2

Linked Data

• dbSNP Id: rs186232310
• MyVariant Identifiers: chr17:g.37881050G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724797G>T , CM000679.2:g.39724797G>T	GRCh38
NC_000017.10:g.37881050G>T , CM000679.1:g.37881050G>T	GRCh37
NC_000017.9:g.35134576G>T	NCBI36
NG_007503.1:g.41658G>T , LRG_724:g.41658G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2379G>T MANE Select	ENSP00000269571.4:p.Thr793=
ENST00000269571.9:c.2379G>T	ENSP00000269571.4:p.Thr793=
ENST00000406381.6:c.2289G>T	ENSP00000385185.2:p.Thr763=
ENST00000445658.6:c.1551G>T	ENSP00000404047.2:p.Thr517=
ENST00000541774.5:c.2334G>T	ENSP00000446466.1:p.Thr778=
ENST00000578373.5:c.*2169G>T	ENSP00000463427.1:n.*2169G>T
ENST00000580074.1:c.485G>T
ENST00000583038.5:n.3513G>T
ENST00000584450.5:c.2379G>T	ENSP00000463714.1:p.Thr793=
ENST00000584601.5:c.2289G>T	ENSP00000462438.1:p.Thr763=
NM_001005862.2:c.2289G>T , LRG_724t1:c.2289G>T	NP_001005862.1:p.Thr763=
NM_001289936.1:c.2334G>T , LRG_724t4:c.2334G>T	NP_001276865.1:p.Thr778=
NM_001289937.1:c.2379G>T	NP_001276866.1:p.Thr793=
NM_004448.3:c.2379G>T , LRG_724t2:c.2379G>T	NP_004439.2:p.Thr793=
NR_110535.1:n.2703G>T
XM_024450641.1:c.2517G>T	XP_024306409.1:p.Thr839=
XM_024450642.1:c.2472G>T	XP_024306410.1:p.Thr824=
XM_024450643.1:c.2427G>T	XP_024306411.1:p.Thr809=
NM_001005862.3:c.2289G>T	NP_001005862.1:p.Thr763=
NM_001289936.2:c.2334G>T	NP_001276865.1:p.Thr778=
NM_001289937.2:c.2379G>T	NP_001276866.1:p.Thr793=
NM_001382782.1:c.2289G>T	NP_001369711.1:p.Thr763=
NM_001382783.1:c.2289G>T	NP_001369712.1:p.Thr763=
NM_001382784.1:c.2496G>T	NP_001369713.1:p.Thr832=
NM_001382785.1:c.2481G>T	NP_001369714.1:p.Thr827=
NM_001382786.1:c.2460G>T	NP_001369715.1:p.Thr820=
NM_001382787.1:c.2454G>T	NP_001369716.1:p.Thr818=
NM_001382788.1:c.2409G>T	NP_001369717.1:p.Thr803=
NM_001382789.1:c.2400G>T	NP_001369718.1:p.Thr800=
NM_001382790.1:c.2376G>T	NP_001369719.1:p.Thr792=
NM_001382791.1:c.2370G>T	NP_001369720.1:p.Thr790=
NM_001382792.1:c.2343G>T	NP_001369721.1:p.Thr781=
NM_001382793.1:c.2337G>T	NP_001369722.1:p.Thr779=
NM_001382794.1:c.2337G>T	NP_001369723.1:p.Thr779=
NM_001382795.1:c.2331G>T	NP_001369724.1:p.Thr777=
NM_001382796.1:c.2379G>T	NP_001369725.1:p.Thr793=
NM_001382797.1:c.2280G>T	NP_001369726.1:p.Thr760=
NM_001382798.1:c.2379G>T	NP_001369727.1:p.Thr793=
NM_001382799.1:c.2199G>T	NP_001369728.1:p.Thr733=
NM_001382800.1:c.2308-252G>T	NP_001369729.1:n.2308-252G>T
NM_001382801.1:c.2331G>T	NP_001369730.1:p.Thr777=
NM_001382802.1:c.2121G>T	NP_001369731.1:p.Thr707=
NM_001382803.1:c.2337G>T	NP_001369732.1:p.Thr779=
NM_001382804.1:c.1551G>T	NP_001369733.1:p.Thr517=
NM_001382805.1:c.2208+1137G>T	NP_001369734.1:n.2208+1137G>T
NM_001382806.1:c.1341G>T	NP_001369735.1:p.Thr447=
NM_004448.4:c.2379G>T MANE Select	NP_004439.2:p.Thr793=
NR_110535.2:n.2617G>T