Canonical Allele Identifier: CA499890124

Gene: ERBB2

Linked Data

• dbSNP Id: rs766022187
• gnomAD v4: 17-39725102-G-C
• MyVariant Identifiers: chr17:g.37881355G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725102G>C , CM000679.2:g.39725102G>C	GRCh38
NC_000017.10:g.37881355G>C , CM000679.1:g.37881355G>C	GRCh37
NC_000017.9:g.35134881G>C	NCBI36
NG_007503.1:g.41963G>C , LRG_724:g.41963G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2547G>C MANE Select	ENSP00000269571.4:p.Arg849=
ENST00000269571.9:c.2547G>C	ENSP00000269571.4:p.Arg849=
ENST00000406381.6:c.2457G>C	ENSP00000385185.2:p.Arg819=
ENST00000445658.6:c.1719G>C	ENSP00000404047.2:p.Arg573=
ENST00000541774.5:c.2502G>C	ENSP00000446466.1:p.Arg834=
ENST00000578373.5:c.*2337G>C	ENSP00000463427.1:n.*2337G>C
ENST00000580074.1:c.653G>C
ENST00000583038.5:n.3681G>C
ENST00000584450.5:c.2547G>C	ENSP00000463714.1:p.Arg849=
ENST00000584601.5:c.2457G>C	ENSP00000462438.1:p.Arg819=
NM_001005862.2:c.2457G>C , LRG_724t1:c.2457G>C	NP_001005862.1:p.Arg819=
NM_001289936.1:c.2502G>C , LRG_724t4:c.2502G>C	NP_001276865.1:p.Arg834=
NM_001289937.1:c.2547G>C	NP_001276866.1:p.Arg849=
NM_004448.3:c.2547G>C , LRG_724t2:c.2547G>C	NP_004439.2:p.Arg849=
NR_110535.1:n.2871G>C
XM_024450641.1:c.2685G>C	XP_024306409.1:p.Arg895=
XM_024450642.1:c.2640G>C	XP_024306410.1:p.Arg880=
XM_024450643.1:c.2595G>C	XP_024306411.1:p.Arg865=
NM_001005862.3:c.2457G>C	NP_001005862.1:p.Arg819=
NM_001289936.2:c.2502G>C	NP_001276865.1:p.Arg834=
NM_001289937.2:c.2547G>C	NP_001276866.1:p.Arg849=
NM_001382782.1:c.2457G>C	NP_001369711.1:p.Arg819=
NM_001382783.1:c.2457G>C	NP_001369712.1:p.Arg819=
NM_001382784.1:c.2664G>C	NP_001369713.1:p.Arg888=
NM_001382785.1:c.2649G>C	NP_001369714.1:p.Arg883=
NM_001382786.1:c.2628G>C	NP_001369715.1:p.Arg876=
NM_001382787.1:c.2622G>C	NP_001369716.1:p.Arg874=
NM_001382788.1:c.2577G>C	NP_001369717.1:p.Arg859=
NM_001382789.1:c.2568G>C	NP_001369718.1:p.Arg856=
NM_001382790.1:c.2544G>C	NP_001369719.1:p.Arg848=
NM_001382791.1:c.2538G>C	NP_001369720.1:p.Arg846=
NM_001382792.1:c.2511G>C	NP_001369721.1:p.Arg837=
NM_001382793.1:c.2505G>C	NP_001369722.1:p.Arg835=
NM_001382794.1:c.2505G>C	NP_001369723.1:p.Arg835=
NM_001382795.1:c.2499G>C	NP_001369724.1:p.Arg833=
NM_001382796.1:c.2547G>C	NP_001369725.1:p.Arg849=
NM_001382797.1:c.2448G>C	NP_001369726.1:p.Arg816=
NM_001382798.1:c.2493+191G>C	NP_001369727.1:n.2493+191G>C
NM_001382799.1:c.2367G>C	NP_001369728.1:p.Arg789=
NM_001382800.1:c.2361G>C	NP_001369729.1:p.Arg787=
NM_001382801.1:c.2445+191G>C	NP_001369730.1:n.2445+191G>C
NM_001382802.1:c.2289G>C	NP_001369731.1:p.Arg763=
NM_001382803.1:c.2505G>C	NP_001369732.1:p.Arg835=
NM_001382804.1:c.1719G>C	NP_001369733.1:p.Arg573=
NM_001382805.1:c.2208+1442G>C	NP_001369734.1:n.2208+1442G>C
NM_001382806.1:c.1509G>C	NP_001369735.1:p.Arg503=
NM_004448.4:c.2547G>C MANE Select	NP_004439.2:p.Arg849=
NR_110535.2:n.2785G>C