Canonical Allele Identifier: CA439489585
Gene: KDR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.55991398A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125231A>G , CM000666.2:g.55125231A>G GRCh38
NC_000004.11:g.55991398A>G , CM000666.1:g.55991398A>G GRCh37
NC_000004.10:g.55686155A>G NCBI36
NG_012004.1:g.5365T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.63T>C MANE Select ENSP00000263923.4:p.Ser21=
ENST00000263923.4:c.63T>C ENSP00000263923.4:p.Ser21=
ENST00000512566.1:n.63T>C
NM_002253.2:c.63T>C NP_002244.1:p.Ser21=
NM_002253.3:c.63T>C NP_002244.1:p.Ser21=
NM_002253.4:c.63T>C MANE Select NP_002244.1:p.Ser21=