Canonical Allele Identifier: CA158663
Gene: ERBB2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 134082
ClinVar RCV Id: RCV000120753
dbSNP Id: rs1058808

User contributed link-outs

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39727784C>G , CM000679.2:g.39727784C>G GRCh38
NC_000017.10:g.37884037C>G , CM000679.1:g.37884037C>G GRCh37
NC_000017.9:g.35137563C>G NCBI36
NG_007503.1:g.44645C>G , LRG_724:g.44645C>G

Transcript Alleles

HGVS Amino-acid change
NM_001005862.2:c.3418C>G , LRG_724t1:c.3418C>G NP_001005862.1:p.Pro1140Ala
NM_001289936.1:c.3463C>G , LRG_724t4:c.3463C>G NP_001276865.1:p.Pro1155Ala
NM_001289937.1:c.*87C>G VV NP_001276866.1:p.=
NM_004448.3:c.3508C>G , LRG_724t2:c.3508C>G NP_004439.2:p.Pro1170Ala
NR_110535.1:n.3832C>G
XM_024450641.1:c.3646C>G XP_024306409.1:p.Pro1216Ala
XM_024450642.1:c.3601C>G XP_024306410.1:p.Pro1201Ala
XM_024450643.1:c.3556C>G XP_024306411.1:p.Pro1186Ala
ENST00000269571.9:c.3508C>G ENSP00000269571.4:p.Pro1170Ala
ENST00000406381.6:c.3418C>G ENSP00000385185.2:p.Pro1140Ala
ENST00000445658.6:c.2680C>G ENSP00000404047.2:p.Pro894Ala
ENST00000541774.5:n.3463C>G ENSP00000446466.1:p.Pro1155Ala
ENST00000578373.5:c.*3298C>G ENSP00000463427.1:p.=
ENST00000584450.5:c.*87C>G ENSP00000463714.1:p.=
ENST00000584601.5:c.3418C>G ENSP00000462438.1:p.Pro1140Ala