LDH info

Canonical Allele Identifier: CA158927306
Gene: EGFR HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs12538371

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.55168327T>C , CM000669.2:g.55168327T>C GRCh38
NC_000007.13:g.55236020T>C , CM000669.1:g.55236020T>C GRCh37
NC_000007.12:g.55203514T>C NCBI36
NG_007726.3:g.154296T>C , LRG_304:g.154296T>C

Transcript Alleles

HGVS Amino-acid change
NM_005228.3:c.1881-2848T>C , LRG_304t1:c.1881-2848T>C NP_005219.2:p.=
NM_201282.1:c.1881-196T>C VV NP_958439.1:p.=
NM_201284.1:c.1881-1980T>C VV NP_958441.1:p.=
NM_001346897.1:c.1746-2848T>C VV NP_001333826.1:p.=
NM_001346898.1:c.1881-2848T>C VV NP_001333827.1:p.=
NM_001346899.1:c.1746-2848T>C VV NP_001333828.1:p.=
NM_001346900.1:c.1722-2848T>C VV NP_001333829.1:p.=
NM_001346941.1:c.1080-2848T>C VV NP_001333870.1:p.=
NM_005228.4:c.1881-2848T>C VV NP_005219.2:p.=
NM_005228.5:c.1881-2848T>C VV MANE Preferred NP_005219.2:p.=
ENST00000275493.6:c.1881-2848T>C ENSP00000275493.2:p.=
ENST00000342916.7:c.1881-196T>C ENSP00000342376.3:p.=
ENST00000344576.6:c.1881-1980T>C ENSP00000345973.2:p.=
ENST00000442591.5:c.1881-2848T>C ENSP00000410031.1:p.=
ENST00000454757.6:c.1746-2848T>C ENSP00000395243.3:p.=
ENST00000455089.5:c.1746-2848T>C ENSP00000415559.1:p.=