LDH info

Canonical Allele Identifier: CA123601
Gene: ERBB2 HGNC NCBI

Identifiers and link-outs to other resources

ClinVar Variation Id: 13880
dbSNP Id: rs28933370
COSMIC: COSM686

User contributed link-outs

CIViC: CA123601

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.39725125A>G , CM000679.2:g.39725125A>G GRCh38
NC_000017.10:g.37881378A>G , CM000679.1:g.37881378A>G GRCh37
NC_000017.9:g.35134904A>G NCBI36
NG_007503.1:g.41986A>G , LRG_724:g.41986A>G

Transcript Alleles

HGVS Amino-acid change
NM_001005862.2:c.2480A>G , LRG_724t1:c.2480A>G NP_001005862.1:p.Asn827Ser
NM_001289936.1:c.2525A>G , LRG_724t4:c.2525A>G NP_001276865.1:p.Asn842Ser
NM_001289937.1:c.2570A>G VV NP_001276866.1:p.Asn857Ser
NM_004448.3:c.2570A>G , LRG_724t2:c.2570A>G NP_004439.2:p.Asn857Ser
NR_110535.1:n.2894A>G
XM_024450641.1:c.2708A>G XP_024306409.1:p.Asn903Ser
XM_024450642.1:c.2663A>G XP_024306410.1:p.Asn888Ser
XM_024450643.1:c.2618A>G XP_024306411.1:p.Asn873Ser
ENST00000269571.9:c.2570A>G ENSP00000269571.4:p.Asn857Ser
ENST00000406381.6:c.2480A>G ENSP00000385185.2:p.Asn827Ser
ENST00000445658.6:c.1742A>G ENSP00000404047.2:p.Asn581Ser
ENST00000541774.5:n.2525A>G ENSP00000446466.1:p.Asn842Ser
ENST00000578373.5:c.*2360A>G ENSP00000463427.1:p.=
ENST00000580074.1:n.676A>G
ENST00000583038.5:n.3704A>G
ENST00000584450.5:c.2570A>G ENSP00000463714.1:p.Asn857Ser
ENST00000584601.5:c.2480A>G ENSP00000462438.1:p.Asn827Ser