Canonical Allele Identifier: CA2706110933
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs2110039078

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125008A>G , CM000666.2:g.55125008A>G GRCh38
NC_000004.11:g.55991175A>G , CM000666.1:g.55991175A>G GRCh37
NC_000004.10:g.55685932A>G NCBI36
NG_012004.1:g.5588T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.67+219T>C MANE Select ENSP00000263923.4:n.67+219T>C
ENST00000263923.4:c.67+219T>C ENSP00000263923.4:n.67+219T>C
ENST00000512566.1:n.67+219T>C
NM_002253.2:c.67+219T>C NP_002244.1:n.67+219T>C
NM_002253.3:c.67+219T>C NP_002244.1:n.67+219T>C
NM_002253.4:c.67+219T>C MANE Select NP_002244.1:n.67+219T>C