Canonical Allele Identifier: CA251259
Gene: KDR HGNC NCBI

Linked Data

ClinVar Variation Id: 204331
ClinVar RCV Id: RCV000186522
dbSNP Id: rs795902897
MyVariant Identifiers: chr4:g.55964284A>T (hg19) chr4:g.55098117A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55098117A>T , CM000666.2:g.55098117A>T GRCh38
NC_000004.11:g.55964284A>T , CM000666.1:g.55964284A>T GRCh37
NC_000004.10:g.55659041A>T NCBI36
NG_012004.1:g.32479T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.2509+20T>A MANE Select ENSP00000263923.4:n.2509+20T>A
ENST00000647068.1:n.2522+20T>A
ENST00000263923.4:c.2509+20T>A ENSP00000263923.4:n.2509+20T>A
NM_002253.2:c.2509+20T>A NP_002244.1:n.2509+20T>A
NM_002253.3:c.2509+20T>A NP_002244.1:n.2509+20T>A
NM_002253.4:c.2509+20T>A MANE Select NP_002244.1:n.2509+20T>A
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