Canonical Allele Identifier: CA399312551

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143252084
• MyVariant Identifiers: chr17:g.37883722T>C (hg19) ; chr17:g.39727469T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727469T>C , CM000679.2:g.39727469T>C	GRCh38
NC_000017.10:g.37883722T>C , CM000679.1:g.37883722T>C	GRCh37
NC_000017.9:g.35137248T>C	NCBI36
NG_007503.1:g.44330T>C , LRG_724:g.44330T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3334T>C MANE Select	ENSP00000269571.4:p.Tyr1112His
ENST00000269571.9:c.3334T>C	ENSP00000269571.4:p.Tyr1112His
ENST00000406381.6:c.3244T>C	ENSP00000385185.2:p.Tyr1082His
ENST00000445658.6:c.2506T>C	ENSP00000404047.2:p.Tyr836His
ENST00000541774.5:c.3289T>C	ENSP00000446466.1:p.Tyr1097His
ENST00000578373.5:c.*3124T>C	ENSP00000463427.1:n.*3124T>C
ENST00000584450.5:c.3160-220T>C	ENSP00000463714.1:n.3160-220T>C
ENST00000584601.5:c.3244T>C	ENSP00000462438.1:p.Tyr1082His
NM_001005862.2:c.3244T>C , LRG_724t1:c.3244T>C	NP_001005862.1:p.Tyr1082His
NM_001289936.1:c.3289T>C , LRG_724t4:c.3289T>C	NP_001276865.1:p.Tyr1097His
NM_001289937.1:c.3160-220T>C	NP_001276866.1:n.3160-220T>C
NM_004448.3:c.3334T>C , LRG_724t2:c.3334T>C	NP_004439.2:p.Tyr1112His
NR_110535.1:n.3658T>C
XM_024450641.1:c.3472T>C	XP_024306409.1:p.Tyr1158His
XM_024450642.1:c.3427T>C	XP_024306410.1:p.Tyr1143His
XM_024450643.1:c.3382T>C	XP_024306411.1:p.Tyr1128His
NM_001005862.3:c.3244T>C	NP_001005862.1:p.Tyr1082His
NM_001289936.2:c.3289T>C	NP_001276865.1:p.Tyr1097His
NM_001289937.2:c.3160-220T>C	NP_001276866.1:n.3160-220T>C
NM_001382782.1:c.3244T>C	NP_001369711.1:p.Tyr1082His
NM_001382783.1:c.3244T>C	NP_001369712.1:p.Tyr1082His
NM_001382784.1:c.3451T>C	NP_001369713.1:p.Tyr1151His
NM_001382785.1:c.3436T>C	NP_001369714.1:p.Tyr1146His
NM_001382786.1:c.3415T>C	NP_001369715.1:p.Tyr1139His
NM_001382787.1:c.3409T>C	NP_001369716.1:p.Tyr1137His
NM_001382788.1:c.3364T>C	NP_001369717.1:p.Tyr1122His
NM_001382789.1:c.3355T>C	NP_001369718.1:p.Tyr1119His
NM_001382790.1:c.3331T>C	NP_001369719.1:p.Tyr1111His
NM_001382791.1:c.3325T>C	NP_001369720.1:p.Tyr1109His
NM_001382792.1:c.3298T>C	NP_001369721.1:p.Tyr1100His
NM_001382793.1:c.3292T>C	NP_001369722.1:p.Tyr1098His
NM_001382794.1:c.3292T>C	NP_001369723.1:p.Tyr1098His
NM_001382795.1:c.3286T>C	NP_001369724.1:p.Tyr1096His
NM_001382796.1:c.3247T>C	NP_001369725.1:p.Tyr1083His
NM_001382797.1:c.3235T>C	NP_001369726.1:p.Tyr1079His
NM_001382798.1:c.3178T>C	NP_001369727.1:p.Tyr1060His
NM_001382799.1:c.3154T>C	NP_001369728.1:p.Tyr1052His
NM_001382800.1:c.3148T>C	NP_001369729.1:p.Tyr1050His
NM_001382801.1:c.3130T>C	NP_001369730.1:p.Tyr1044His
NM_001382802.1:c.3076T>C	NP_001369731.1:p.Tyr1026His
NM_001382803.1:c.3118-220T>C	NP_001369732.1:n.3118-220T>C
NM_001382804.1:c.2506T>C	NP_001369733.1:p.Tyr836His
NM_001382805.1:c.2383T>C	NP_001369734.1:p.Tyr795His
NM_001382806.1:c.2296T>C	NP_001369735.1:p.Tyr766His
NM_004448.4:c.3334T>C MANE Select	NP_004439.2:p.Tyr1112His
NR_110535.2:n.3572T>C