Canonical Allele Identifier: CA439489599
Gene: KDR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.55991413C>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125246C>T , CM000666.2:g.55125246C>T GRCh38
NC_000004.11:g.55991413C>T , CM000666.1:g.55991413C>T GRCh37
NC_000004.10:g.55686170C>T NCBI36
NG_012004.1:g.5350G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.48G>A MANE Select ENSP00000263923.4:p.Glu16=
ENST00000263923.4:c.48G>A ENSP00000263923.4:p.Glu16=
ENST00000512566.1:n.48G>A
NM_002253.2:c.48G>A NP_002244.1:p.Glu16=
NM_002253.3:c.48G>A NP_002244.1:p.Glu16=
NM_002253.4:c.48G>A MANE Select NP_002244.1:p.Glu16=