Canonical Allele Identifier: CA251253
Gene: KDR HGNC NCBI

Linked Data

ClinVar Variation Id: 204328
ClinVar RCV Id: RCV000186519
dbSNP Id: rs794729678
MyVariant Identifiers: chr4:g.55962419A>T (hg19) chr4:g.55096252A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55096252A>T , CM000666.2:g.55096252A>T GRCh38
NC_000004.11:g.55962419A>T , CM000666.1:g.55962419A>T GRCh37
NC_000004.10:g.55657176A>T NCBI36
NG_012004.1:g.34344T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.2705T>A MANE Select ENSP00000263923.4:p.Leu902Gln
ENST00000647068.1:n.2718T>A
ENST00000263923.4:c.2705T>A ENSP00000263923.4:p.Leu902Gln
ENST00000509309.1:n.469T>A
NM_002253.2:c.2705T>A NP_002244.1:p.Leu902Gln
NM_002253.3:c.2705T>A NP_002244.1:p.Leu902Gln
NM_002253.4:c.2705T>A MANE Select NP_002244.1:p.Leu902Gln
Search 100 bp 5'
Search 100 bp 3'