Canonical Allele Identifier: CA163008
Gene: KDR HGNC NCBI

Linked Data

ClinVar Variation Id: 135551
ClinVar RCV Id: RCV000122411
dbSNP Id: rs17085310
ExAC: 4:55970782 G / A
gnomAD v2: 4-55970782-G-A
gnomAD v3: 4-55104615-G-A
gnomAD v4: 4-55104615-G-A
MyVariant Identifiers: chr4:g.55970782G>A (hg19) chr4:g.55104615G>A (hg38)
PubMed: PMID:24728327
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55104615G>A , CM000666.2:g.55104615G>A GRCh38
NC_000004.11:g.55970782G>A , CM000666.1:g.55970782G>A GRCh37
NC_000004.10:g.55665539G>A NCBI36
NG_012004.1:g.25981C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1987+28C>T MANE Select ENSP00000263923.4:n.1987+28C>T
ENST00000647068.1:n.2000+28C>T
ENST00000263923.4:c.1987+28C>T ENSP00000263923.4:n.1987+28C>T
ENST00000512566.1:n.2015C>T
NM_002253.2:c.1987+28C>T NP_002244.1:n.1987+28C>T
NM_002253.3:c.1987+28C>T NP_002244.1:n.1987+28C>T
NM_002253.4:c.1987+28C>T MANE Select NP_002244.1:n.1987+28C>T
Search 100 bp 5'
Search 100 bp 3'