Canonical Allele Identifier: CA2259229167

Gene: ERBB2

Linked Data

• dbSNP Id: rs2059846558
• gnomAD v4: 17-39727576-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727576T>C , CM000679.2:g.39727576T>C	GRCh38
NC_000017.10:g.37883829T>C , CM000679.1:g.37883829T>C	GRCh37
NC_000017.9:g.35137355T>C	NCBI36
NG_007503.1:g.44437T>C , LRG_724:g.44437T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3412+29T>C MANE Select	ENSP00000269571.4:n.3412+29T>C
ENST00000269571.9:c.3412+29T>C	ENSP00000269571.4:n.3412+29T>C
ENST00000406381.6:c.3322+29T>C	ENSP00000385185.2:n.3322+29T>C
ENST00000445658.6:c.2584+29T>C	ENSP00000404047.2:n.2584+29T>C
ENST00000541774.5:c.3367+29T>C	ENSP00000446466.1:n.3367+29T>C
ENST00000578373.5:c.*3202+29T>C	ENSP00000463427.1:n.*3202+29T>C
ENST00000584450.5:c.3160-113T>C	ENSP00000463714.1:n.3160-113T>C
ENST00000584601.5:c.3322+29T>C	ENSP00000462438.1:n.3322+29T>C
NM_001005862.2:c.3322+29T>C , LRG_724t1:c.3322+29T>C	NP_001005862.1:n.3322+29T>C
NM_001289936.1:c.3367+29T>C , LRG_724t4:c.3367+29T>C	NP_001276865.1:n.3367+29T>C
NM_001289937.1:c.3160-113T>C	NP_001276866.1:n.3160-113T>C
NM_004448.3:c.3412+29T>C , LRG_724t2:c.3412+29T>C	NP_004439.2:n.3412+29T>C
NR_110535.1:n.3736+29T>C
XM_024450641.1:c.3550+29T>C	XP_024306409.1:n.3550+29T>C
XM_024450642.1:c.3505+29T>C	XP_024306410.1:n.3505+29T>C
XM_024450643.1:c.3460+29T>C	XP_024306411.1:n.3460+29T>C
NM_001005862.3:c.3322+29T>C	NP_001005862.1:n.3322+29T>C
NM_001289936.2:c.3367+29T>C	NP_001276865.1:n.3367+29T>C
NM_001289937.2:c.3160-113T>C	NP_001276866.1:n.3160-113T>C
NM_001382782.1:c.3322+29T>C	NP_001369711.1:n.3322+29T>C
NM_001382783.1:c.3322+29T>C	NP_001369712.1:n.3322+29T>C
NM_001382784.1:c.3529+29T>C	NP_001369713.1:n.3529+29T>C
NM_001382785.1:c.3514+29T>C	NP_001369714.1:n.3514+29T>C
NM_001382786.1:c.3493+29T>C	NP_001369715.1:n.3493+29T>C
NM_001382787.1:c.3487+29T>C	NP_001369716.1:n.3487+29T>C
NM_001382788.1:c.3442+29T>C	NP_001369717.1:n.3442+29T>C
NM_001382789.1:c.3433+29T>C	NP_001369718.1:n.3433+29T>C
NM_001382790.1:c.3409+29T>C	NP_001369719.1:n.3409+29T>C
NM_001382791.1:c.3403+29T>C	NP_001369720.1:n.3403+29T>C
NM_001382792.1:c.3376+29T>C	NP_001369721.1:n.3376+29T>C
NM_001382793.1:c.3370+29T>C	NP_001369722.1:n.3370+29T>C
NM_001382794.1:c.3370+29T>C	NP_001369723.1:n.3370+29T>C
NM_001382795.1:c.3364+29T>C	NP_001369724.1:n.3364+29T>C
NM_001382796.1:c.3325+29T>C	NP_001369725.1:n.3325+29T>C
NM_001382797.1:c.3313+29T>C	NP_001369726.1:n.3313+29T>C
NM_001382798.1:c.3256+29T>C	NP_001369727.1:n.3256+29T>C
NM_001382799.1:c.3232+29T>C	NP_001369728.1:n.3232+29T>C
NM_001382800.1:c.3226+29T>C	NP_001369729.1:n.3226+29T>C
NM_001382801.1:c.3208+29T>C	NP_001369730.1:n.3208+29T>C
NM_001382802.1:c.3154+29T>C	NP_001369731.1:n.3154+29T>C
NM_001382803.1:c.3118-113T>C	NP_001369732.1:n.3118-113T>C
NM_001382804.1:c.2584+29T>C	NP_001369733.1:n.2584+29T>C
NM_001382805.1:c.2461+29T>C	NP_001369734.1:n.2461+29T>C
NM_001382806.1:c.2374+29T>C	NP_001369735.1:n.2374+29T>C
NM_004448.4:c.3412+29T>C MANE Select	NP_004439.2:n.3412+29T>C
NR_110535.2:n.3650+29T>C