Canonical Allele Identifier: CA356921469
Gene: KDR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.55991429A>C (hg19) chr4:g.55125262A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125262A>C , CM000666.2:g.55125262A>C GRCh38
NC_000004.11:g.55991429A>C , CM000666.1:g.55991429A>C GRCh37
NC_000004.10:g.55686186A>C NCBI36
NG_012004.1:g.5334T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.32T>G MANE Select ENSP00000263923.4:p.Leu11Arg
ENST00000263923.4:c.32T>G ENSP00000263923.4:p.Leu11Arg
ENST00000512566.1:n.32T>G
NM_002253.2:c.32T>G NP_002244.1:p.Leu11Arg
NM_002253.3:c.32T>G NP_002244.1:p.Leu11Arg
NM_002253.4:c.32T>G MANE Select NP_002244.1:p.Leu11Arg
Search 100 bp 5'
Search 100 bp 3'