Canonical Allele Identifier: CA499670881

Gene: ERBB2

Linked Data

• dbSNP Id: rs2145849738
• MyVariant Identifiers: chr17:g.37881047C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39724794C>G , CM000679.2:g.39724794C>G	GRCh38
NC_000017.10:g.37881047C>G , CM000679.1:g.37881047C>G	GRCh37
NC_000017.9:g.35134573C>G	NCBI36
NG_007503.1:g.41655C>G , LRG_724:g.41655C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.2376C>G MANE Select	ENSP00000269571.4:p.Ser792=
ENST00000269571.9:c.2376C>G	ENSP00000269571.4:p.Ser792=
ENST00000406381.6:c.2286C>G	ENSP00000385185.2:p.Ser762=
ENST00000445658.6:c.1548C>G	ENSP00000404047.2:p.Ser516=
ENST00000541774.5:c.2331C>G	ENSP00000446466.1:p.Ser777=
ENST00000578373.5:c.*2166C>G	ENSP00000463427.1:n.*2166C>G
ENST00000580074.1:c.482C>G
ENST00000583038.5:n.3510C>G
ENST00000584450.5:c.2376C>G	ENSP00000463714.1:p.Ser792=
ENST00000584601.5:c.2286C>G	ENSP00000462438.1:p.Ser762=
NM_001005862.2:c.2286C>G , LRG_724t1:c.2286C>G	NP_001005862.1:p.Ser762=
NM_001289936.1:c.2331C>G , LRG_724t4:c.2331C>G	NP_001276865.1:p.Ser777=
NM_001289937.1:c.2376C>G	NP_001276866.1:p.Ser792=
NM_004448.3:c.2376C>G , LRG_724t2:c.2376C>G	NP_004439.2:p.Ser792=
NR_110535.1:n.2700C>G
XM_024450641.1:c.2514C>G	XP_024306409.1:p.Ser838=
XM_024450642.1:c.2469C>G	XP_024306410.1:p.Ser823=
XM_024450643.1:c.2424C>G	XP_024306411.1:p.Ser808=
NM_001005862.3:c.2286C>G	NP_001005862.1:p.Ser762=
NM_001289936.2:c.2331C>G	NP_001276865.1:p.Ser777=
NM_001289937.2:c.2376C>G	NP_001276866.1:p.Ser792=
NM_001382782.1:c.2286C>G	NP_001369711.1:p.Ser762=
NM_001382783.1:c.2286C>G	NP_001369712.1:p.Ser762=
NM_001382784.1:c.2493C>G	NP_001369713.1:p.Ser831=
NM_001382785.1:c.2478C>G	NP_001369714.1:p.Ser826=
NM_001382786.1:c.2457C>G	NP_001369715.1:p.Ser819=
NM_001382787.1:c.2451C>G	NP_001369716.1:p.Ser817=
NM_001382788.1:c.2406C>G	NP_001369717.1:p.Ser802=
NM_001382789.1:c.2397C>G	NP_001369718.1:p.Ser799=
NM_001382790.1:c.2373C>G	NP_001369719.1:p.Ser791=
NM_001382791.1:c.2367C>G	NP_001369720.1:p.Ser789=
NM_001382792.1:c.2340C>G	NP_001369721.1:p.Ser780=
NM_001382793.1:c.2334C>G	NP_001369722.1:p.Ser778=
NM_001382794.1:c.2334C>G	NP_001369723.1:p.Ser778=
NM_001382795.1:c.2328C>G	NP_001369724.1:p.Ser776=
NM_001382796.1:c.2376C>G	NP_001369725.1:p.Ser792=
NM_001382797.1:c.2277C>G	NP_001369726.1:p.Ser759=
NM_001382798.1:c.2376C>G	NP_001369727.1:p.Ser792=
NM_001382799.1:c.2196C>G	NP_001369728.1:p.Ser732=
NM_001382800.1:c.2308-255C>G	NP_001369729.1:n.2308-255C>G
NM_001382801.1:c.2328C>G	NP_001369730.1:p.Ser776=
NM_001382802.1:c.2118C>G	NP_001369731.1:p.Ser706=
NM_001382803.1:c.2334C>G	NP_001369732.1:p.Ser778=
NM_001382804.1:c.1548C>G	NP_001369733.1:p.Ser516=
NM_001382805.1:c.2208+1134C>G	NP_001369734.1:n.2208+1134C>G
NM_001382806.1:c.1338C>G	NP_001369735.1:p.Ser446=
NM_004448.4:c.2376C>G MANE Select	NP_004439.2:p.Ser792=
NR_110535.2:n.2614C>G