Canonical Allele Identifier: CA499890863

Gene: ERBB2

Linked Data

• dbSNP Id: rs2143313082
• MyVariant Identifiers: chr17:g.37884192T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.39727939T>C , CM000679.2:g.39727939T>C	GRCh38
NC_000017.10:g.37884192T>C , CM000679.1:g.37884192T>C	GRCh37
NC_000017.9:g.35137718T>C	NCBI36
NG_007503.1:g.44800T>C , LRG_724:g.44800T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000269571.10:c.3663T>C MANE Select	ENSP00000269571.4:p.Tyr1221=
ENST00000269571.9:c.3663T>C	ENSP00000269571.4:p.Tyr1221=
ENST00000406381.6:c.3573T>C	ENSP00000385185.2:p.Tyr1191=
ENST00000445658.6:c.2835T>C	ENSP00000404047.2:p.Tyr945=
ENST00000541774.5:c.3618T>C	ENSP00000446466.1:p.Tyr1206=
ENST00000578373.5:c.*3453T>C	ENSP00000463427.1:n.*3453T>C
ENST00000584450.5:c.*242T>C	ENSP00000463714.1:n.*242T>C
ENST00000584601.5:c.3573T>C	ENSP00000462438.1:p.Tyr1191=
NM_001005862.2:c.3573T>C , LRG_724t1:c.3573T>C	NP_001005862.1:p.Tyr1191=
NM_001289936.1:c.3618T>C , LRG_724t4:c.3618T>C	NP_001276865.1:p.Tyr1206=
NM_001289937.1:c.*242T>C	NP_001276866.1:n.*242T>C
NM_004448.3:c.3663T>C , LRG_724t2:c.3663T>C	NP_004439.2:p.Tyr1221=
NR_110535.1:n.3987T>C
XM_024450641.1:c.3801T>C	XP_024306409.1:p.Tyr1267=
XM_024450642.1:c.3756T>C	XP_024306410.1:p.Tyr1252=
XM_024450643.1:c.3711T>C	XP_024306411.1:p.Tyr1237=
NM_001005862.3:c.3573T>C	NP_001005862.1:p.Tyr1191=
NM_001289936.2:c.3618T>C	NP_001276865.1:p.Tyr1206=
NM_001289937.2:c.*242T>C	NP_001276866.1:n.*242T>C
NM_001382782.1:c.3573T>C	NP_001369711.1:p.Tyr1191=
NM_001382783.1:c.3573T>C	NP_001369712.1:p.Tyr1191=
NM_001382784.1:c.3780T>C	NP_001369713.1:p.Tyr1260=
NM_001382785.1:c.3765T>C	NP_001369714.1:p.Tyr1255=
NM_001382786.1:c.3744T>C	NP_001369715.1:p.Tyr1248=
NM_001382787.1:c.3738T>C	NP_001369716.1:p.Tyr1246=
NM_001382788.1:c.3693T>C	NP_001369717.1:p.Tyr1231=
NM_001382789.1:c.3684T>C	NP_001369718.1:p.Tyr1228=
NM_001382790.1:c.3660T>C	NP_001369719.1:p.Tyr1220=
NM_001382791.1:c.3654T>C	NP_001369720.1:p.Tyr1218=
NM_001382792.1:c.3627T>C	NP_001369721.1:p.Tyr1209=
NM_001382793.1:c.3621T>C	NP_001369722.1:p.Tyr1207=
NM_001382794.1:c.3621T>C	NP_001369723.1:p.Tyr1207=
NM_001382795.1:c.3615T>C	NP_001369724.1:p.Tyr1205=
NM_001382796.1:c.3576T>C	NP_001369725.1:p.Tyr1192=
NM_001382797.1:c.3564T>C	NP_001369726.1:p.Tyr1188=
NM_001382798.1:c.3507T>C	NP_001369727.1:p.Tyr1169=
NM_001382799.1:c.3483T>C	NP_001369728.1:p.Tyr1161=
NM_001382800.1:c.3477T>C	NP_001369729.1:p.Tyr1159=
NM_001382801.1:c.3459T>C	NP_001369730.1:p.Tyr1153=
NM_001382802.1:c.3405T>C	NP_001369731.1:p.Tyr1135=
NM_001382803.1:c.*242T>C	NP_001369732.1:n.*242T>C
NM_001382804.1:c.2835T>C	NP_001369733.1:p.Tyr945=
NM_001382805.1:c.2712T>C	NP_001369734.1:p.Tyr904=
NM_001382806.1:c.2625T>C	NP_001369735.1:p.Tyr875=
NM_004448.4:c.3663T>C MANE Select	NP_004439.2:p.Tyr1221=
NR_110535.2:n.3901T>C