Canonical Allele Identifier: CA96921338
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs764580753
MyVariant Identifiers: chr4:g.55991200G>A (hg19) chr4:g.55125033G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125033G>A , CM000666.2:g.55125033G>A GRCh38
NC_000004.11:g.55991200G>A , CM000666.1:g.55991200G>A GRCh37
NC_000004.10:g.55685957G>A NCBI36
NG_012004.1:g.5563C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.67+194C>T MANE Select ENSP00000263923.4:n.67+194C>T
ENST00000263923.4:c.67+194C>T ENSP00000263923.4:n.67+194C>T
ENST00000512566.1:n.67+194C>T
NM_002253.2:c.67+194C>T NP_002244.1:n.67+194C>T
NM_002253.3:c.67+194C>T NP_002244.1:n.67+194C>T
NM_002253.4:c.67+194C>T MANE Select NP_002244.1:n.67+194C>T
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