Canonical Allele Identifier: CA356913477
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs2110028011

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55110703C>A , CM000666.2:g.55110703C>A GRCh38
NC_000004.11:g.55976870C>A , CM000666.1:g.55976870C>A GRCh37
NC_000004.10:g.55671627C>A NCBI36
NG_012004.1:g.19893G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1042G>T MANE Select ENSP00000263923.4:p.Val348Phe
ENST00000647068.1:n.1055G>T
ENST00000263923.4:c.1042G>T ENSP00000263923.4:p.Val348Phe
ENST00000512566.1:n.1042G>T
NM_002253.2:c.1042G>T NP_002244.1:p.Val348Phe
NM_002253.3:c.1042G>T NP_002244.1:p.Val348Phe
NM_002253.4:c.1042G>T MANE Select NP_002244.1:p.Val348Phe