Canonical Allele Identifier: CA290440856

Gene: ERBB2

Linked Data

• dbSNP Id: rs372773414
• gnomAD v4: 17-39725038-T-C
• MyVariant Identifiers: chr17:g.37881291T>C (hg19) ; chr17:g.39725038T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39725038T>C , CM000679.2:g.39725038T>C	GRCh38
NC_000017.10:g.37881291T>C , CM000679.1:g.37881291T>C	GRCh37
NC_000017.9:g.35134817T>C	NCBI36
NG_007503.1:g.41899T>C , LRG_724:g.41899T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000269571.10:c.2494-11T>C MANE Select	ENSP00000269571.4:n.2494-11T>C
ENST00000269571.9:c.2494-11T>C	ENSP00000269571.4:n.2494-11T>C
ENST00000406381.6:c.2404-11T>C	ENSP00000385185.2:n.2404-11T>C
ENST00000445658.6:c.1666-11T>C	ENSP00000404047.2:n.1666-11T>C
ENST00000541774.5:c.2449-11T>C	ENSP00000446466.1:n.2449-11T>C
ENST00000578373.5:c.*2284-11T>C	ENSP00000463427.1:n.*2284-11T>C
ENST00000580074.1:c.600-11T>C
ENST00000583038.5:n.3628-11T>C
ENST00000584450.5:c.2494-11T>C	ENSP00000463714.1:n.2494-11T>C
ENST00000584601.5:c.2404-11T>C	ENSP00000462438.1:n.2404-11T>C
NM_001005862.2:c.2404-11T>C , LRG_724t1:c.2404-11T>C	NP_001005862.1:n.2404-11T>C
NM_001289936.1:c.2449-11T>C , LRG_724t4:c.2449-11T>C	NP_001276865.1:n.2449-11T>C
NM_001289937.1:c.2494-11T>C	NP_001276866.1:n.2494-11T>C
NM_004448.3:c.2494-11T>C , LRG_724t2:c.2494-11T>C	NP_004439.2:n.2494-11T>C
NR_110535.1:n.2818-11T>C
XM_024450641.1:c.2632-11T>C	XP_024306409.1:n.2632-11T>C
XM_024450642.1:c.2587-11T>C	XP_024306410.1:n.2587-11T>C
XM_024450643.1:c.2542-11T>C	XP_024306411.1:n.2542-11T>C
NM_001005862.3:c.2404-11T>C	NP_001005862.1:n.2404-11T>C
NM_001289936.2:c.2449-11T>C	NP_001276865.1:n.2449-11T>C
NM_001289937.2:c.2494-11T>C	NP_001276866.1:n.2494-11T>C
NM_001382782.1:c.2404-11T>C	NP_001369711.1:n.2404-11T>C
NM_001382783.1:c.2404-11T>C	NP_001369712.1:n.2404-11T>C
NM_001382784.1:c.2611-11T>C	NP_001369713.1:n.2611-11T>C
NM_001382785.1:c.2596-11T>C	NP_001369714.1:n.2596-11T>C
NM_001382786.1:c.2575-11T>C	NP_001369715.1:n.2575-11T>C
NM_001382787.1:c.2569-11T>C	NP_001369716.1:n.2569-11T>C
NM_001382788.1:c.2524-11T>C	NP_001369717.1:n.2524-11T>C
NM_001382789.1:c.2515-11T>C	NP_001369718.1:n.2515-11T>C
NM_001382790.1:c.2491-11T>C	NP_001369719.1:n.2491-11T>C
NM_001382791.1:c.2485-11T>C	NP_001369720.1:n.2485-11T>C
NM_001382792.1:c.2458-11T>C	NP_001369721.1:n.2458-11T>C
NM_001382793.1:c.2452-11T>C	NP_001369722.1:n.2452-11T>C
NM_001382794.1:c.2452-11T>C	NP_001369723.1:n.2452-11T>C
NM_001382795.1:c.2446-11T>C	NP_001369724.1:n.2446-11T>C
NM_001382796.1:c.2494-11T>C	NP_001369725.1:n.2494-11T>C
NM_001382797.1:c.2395-11T>C	NP_001369726.1:n.2395-11T>C
NM_001382798.1:c.2493+127T>C	NP_001369727.1:n.2493+127T>C
NM_001382799.1:c.2314-11T>C	NP_001369728.1:n.2314-11T>C
NM_001382800.1:c.2308-11T>C	NP_001369729.1:n.2308-11T>C
NM_001382801.1:c.2445+127T>C	NP_001369730.1:n.2445+127T>C
NM_001382802.1:c.2236-11T>C	NP_001369731.1:n.2236-11T>C
NM_001382803.1:c.2452-11T>C	NP_001369732.1:n.2452-11T>C
NM_001382804.1:c.1666-11T>C	NP_001369733.1:n.1666-11T>C
NM_001382805.1:c.2208+1378T>C	NP_001369734.1:n.2208+1378T>C
NM_001382806.1:c.1456-11T>C	NP_001369735.1:n.1456-11T>C
NM_004448.4:c.2494-11T>C MANE Select	NP_004439.2:n.2494-11T>C
NR_110535.2:n.2732-11T>C