Canonical Allele Identifier: CA499670848

Gene: ERBB2

Linked Data

• dbSNP Id: rs762733948
• MyVariant Identifiers: chr17:g.37881008C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724755C>G , CM000679.2:g.39724755C>G	GRCh38
NC_000017.10:g.37881008C>G , CM000679.1:g.37881008C>G	GRCh37
NC_000017.9:g.35134534C>G	NCBI36
NG_007503.1:g.41616C>G , LRG_724:g.41616C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2337C>G MANE Select	ENSP00000269571.4:p.Ser779=
ENST00000269571.9:c.2337C>G	ENSP00000269571.4:p.Ser779=
ENST00000406381.6:c.2247C>G	ENSP00000385185.2:p.Ser749=
ENST00000445658.6:c.1509C>G	ENSP00000404047.2:p.Ser503=
ENST00000541774.5:c.2292C>G	ENSP00000446466.1:p.Ser764=
ENST00000578373.5:c.*2127C>G	ENSP00000463427.1:n.*2127C>G
ENST00000580074.1:c.443C>G
ENST00000583038.5:n.3471C>G
ENST00000584450.5:c.2337C>G	ENSP00000463714.1:p.Ser779=
ENST00000584601.5:c.2247C>G	ENSP00000462438.1:p.Ser749=
NM_001005862.2:c.2247C>G , LRG_724t1:c.2247C>G	NP_001005862.1:p.Ser749=
NM_001289936.1:c.2292C>G , LRG_724t4:c.2292C>G	NP_001276865.1:p.Ser764=
NM_001289937.1:c.2337C>G	NP_001276866.1:p.Ser779=
NM_004448.3:c.2337C>G , LRG_724t2:c.2337C>G	NP_004439.2:p.Ser779=
NR_110535.1:n.2661C>G
XM_024450641.1:c.2475C>G	XP_024306409.1:p.Ser825=
XM_024450642.1:c.2430C>G	XP_024306410.1:p.Ser810=
XM_024450643.1:c.2385C>G	XP_024306411.1:p.Ser795=
NM_001005862.3:c.2247C>G	NP_001005862.1:p.Ser749=
NM_001289936.2:c.2292C>G	NP_001276865.1:p.Ser764=
NM_001289937.2:c.2337C>G	NP_001276866.1:p.Ser779=
NM_001382782.1:c.2247C>G	NP_001369711.1:p.Ser749=
NM_001382783.1:c.2247C>G	NP_001369712.1:p.Ser749=
NM_001382784.1:c.2454C>G	NP_001369713.1:p.Ser818=
NM_001382785.1:c.2439C>G	NP_001369714.1:p.Ser813=
NM_001382786.1:c.2418C>G	NP_001369715.1:p.Ser806=
NM_001382787.1:c.2412C>G	NP_001369716.1:p.Ser804=
NM_001382788.1:c.2367C>G	NP_001369717.1:p.Ser789=
NM_001382789.1:c.2358C>G	NP_001369718.1:p.Ser786=
NM_001382790.1:c.2334C>G	NP_001369719.1:p.Ser778=
NM_001382791.1:c.2328C>G	NP_001369720.1:p.Ser776=
NM_001382792.1:c.2301C>G	NP_001369721.1:p.Ser767=
NM_001382793.1:c.2295C>G	NP_001369722.1:p.Ser765=
NM_001382794.1:c.2295C>G	NP_001369723.1:p.Ser765=
NM_001382795.1:c.2289C>G	NP_001369724.1:p.Ser763=
NM_001382796.1:c.2337C>G	NP_001369725.1:p.Ser779=
NM_001382797.1:c.2238C>G	NP_001369726.1:p.Ser746=
NM_001382798.1:c.2337C>G	NP_001369727.1:p.Ser779=
NM_001382799.1:c.2157C>G	NP_001369728.1:p.Ser719=
NM_001382800.1:c.2308-294C>G	NP_001369729.1:n.2308-294C>G
NM_001382801.1:c.2289C>G	NP_001369730.1:p.Ser763=
NM_001382802.1:c.2079C>G	NP_001369731.1:p.Ser693=
NM_001382803.1:c.2295C>G	NP_001369732.1:p.Ser765=
NM_001382804.1:c.1509C>G	NP_001369733.1:p.Ser503=
NM_001382805.1:c.2208+1095C>G	NP_001369734.1:n.2208+1095C>G
NM_001382806.1:c.1299C>G	NP_001369735.1:p.Ser433=
NM_004448.4:c.2337C>G MANE Select	NP_004439.2:p.Ser779=
NR_110535.2:n.2575C>G