Canonical Allele Identifier: CA356913478
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs2110028011
MyVariant Identifiers: chr4:g.55976870C>G (hg19) chr4:g.55110703C>G (hg38)
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Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1042G>C MANE Select ENSP00000263923.4:p.Val348Leu
ENST00000647068.1:n.1055G>C
ENST00000263923.4:c.1042G>C ENSP00000263923.4:p.Val348Leu
ENST00000512566.1:n.1042G>C
NM_002253.2:c.1042G>C NP_002244.1:p.Val348Leu
NM_002253.3:c.1042G>C NP_002244.1:p.Val348Leu
NM_002253.4:c.1042G>C MANE Select NP_002244.1:p.Val348Leu
Search 100 bp 5'
Search 100 bp 3'