Canonical Allele Identifier: CA96891315
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs778504307
MyVariant Identifiers: chr4:g.55962539T>A (hg19) chr4:g.55096372T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55096372T>A , CM000666.2:g.55096372T>A GRCh38
NC_000004.11:g.55962539T>A , CM000666.1:g.55962539T>A GRCh37
NC_000004.10:g.55657296T>A NCBI36
NG_012004.1:g.34224A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.2615-30A>T MANE Select ENSP00000263923.4:n.2615-30A>T
ENST00000647068.1:n.2628-30A>T
ENST00000263923.4:c.2615-30A>T ENSP00000263923.4:n.2615-30A>T
ENST00000509309.1:n.349A>T
NM_002253.2:c.2615-30A>T NP_002244.1:n.2615-30A>T
NM_002253.3:c.2615-30A>T NP_002244.1:n.2615-30A>T
NM_002253.4:c.2615-30A>T MANE Select NP_002244.1:n.2615-30A>T
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