Canonical Allele Identifier: CA399312923

Gene: ERBB2

Linked Data

• dbSNP Id: rs751372943
• gnomAD v2: 17-37883992-G-C
• gnomAD v4: 17-39727739-G-C
• MyVariant Identifiers: chr17:g.37883992G>C (hg19) ; chr17:g.39727739G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727739G>C , CM000679.2:g.39727739G>C	GRCh38
NC_000017.10:g.37883992G>C , CM000679.1:g.37883992G>C	GRCh37
NC_000017.9:g.35137518G>C	NCBI36
NG_007503.1:g.44600G>C , LRG_724:g.44600G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3463G>C MANE Select	ENSP00000269571.4:p.Gly1155Arg
ENST00000269571.9:c.3463G>C	ENSP00000269571.4:p.Gly1155Arg
ENST00000406381.6:c.3373G>C	ENSP00000385185.2:p.Gly1125Arg
ENST00000445658.6:c.2635G>C	ENSP00000404047.2:p.Gly879Arg
ENST00000541774.5:c.3418G>C	ENSP00000446466.1:p.Gly1140Arg
ENST00000578373.5:c.*3253G>C	ENSP00000463427.1:n.*3253G>C
ENST00000584450.5:c.*42G>C	ENSP00000463714.1:n.*42G>C
ENST00000584601.5:c.3373G>C	ENSP00000462438.1:p.Gly1125Arg
NM_001005862.2:c.3373G>C , LRG_724t1:c.3373G>C	NP_001005862.1:p.Gly1125Arg
NM_001289936.1:c.3418G>C , LRG_724t4:c.3418G>C	NP_001276865.1:p.Gly1140Arg
NM_001289937.1:c.*42G>C	NP_001276866.1:n.*42G>C
NM_004448.3:c.3463G>C , LRG_724t2:c.3463G>C	NP_004439.2:p.Gly1155Arg
NR_110535.1:n.3787G>C
XM_024450641.1:c.3601G>C	XP_024306409.1:p.Gly1201Arg
XM_024450642.1:c.3556G>C	XP_024306410.1:p.Gly1186Arg
XM_024450643.1:c.3511G>C	XP_024306411.1:p.Gly1171Arg
NM_001005862.3:c.3373G>C	NP_001005862.1:p.Gly1125Arg
NM_001289936.2:c.3418G>C	NP_001276865.1:p.Gly1140Arg
NM_001289937.2:c.*42G>C	NP_001276866.1:n.*42G>C
NM_001382782.1:c.3373G>C	NP_001369711.1:p.Gly1125Arg
NM_001382783.1:c.3373G>C	NP_001369712.1:p.Gly1125Arg
NM_001382784.1:c.3580G>C	NP_001369713.1:p.Gly1194Arg
NM_001382785.1:c.3565G>C	NP_001369714.1:p.Gly1189Arg
NM_001382786.1:c.3544G>C	NP_001369715.1:p.Gly1182Arg
NM_001382787.1:c.3538G>C	NP_001369716.1:p.Gly1180Arg
NM_001382788.1:c.3493G>C	NP_001369717.1:p.Gly1165Arg
NM_001382789.1:c.3484G>C	NP_001369718.1:p.Gly1162Arg
NM_001382790.1:c.3460G>C	NP_001369719.1:p.Gly1154Arg
NM_001382791.1:c.3454G>C	NP_001369720.1:p.Gly1152Arg
NM_001382792.1:c.3427G>C	NP_001369721.1:p.Gly1143Arg
NM_001382793.1:c.3421G>C	NP_001369722.1:p.Gly1141Arg
NM_001382794.1:c.3421G>C	NP_001369723.1:p.Gly1141Arg
NM_001382795.1:c.3415G>C	NP_001369724.1:p.Gly1139Arg
NM_001382796.1:c.3376G>C	NP_001369725.1:p.Gly1126Arg
NM_001382797.1:c.3364G>C	NP_001369726.1:p.Gly1122Arg
NM_001382798.1:c.3307G>C	NP_001369727.1:p.Gly1103Arg
NM_001382799.1:c.3283G>C	NP_001369728.1:p.Gly1095Arg
NM_001382800.1:c.3277G>C	NP_001369729.1:p.Gly1093Arg
NM_001382801.1:c.3259G>C	NP_001369730.1:p.Gly1087Arg
NM_001382802.1:c.3205G>C	NP_001369731.1:p.Gly1069Arg
NM_001382803.1:c.*42G>C	NP_001369732.1:n.*42G>C
NM_001382804.1:c.2635G>C	NP_001369733.1:p.Gly879Arg
NM_001382805.1:c.2512G>C	NP_001369734.1:p.Gly838Arg
NM_001382806.1:c.2425G>C	NP_001369735.1:p.Gly809Arg
NM_004448.4:c.3463G>C MANE Select	NP_004439.2:p.Gly1155Arg
NR_110535.2:n.3701G>C