Canonical Allele Identifier: CA16618047
Gene: KDR HGNC NCBI

Linked Data

ClinVar Variation Id: 423599
ClinVar RCV Id: RCV000483185
dbSNP Id: rs1037612393
gnomAD v2: 4-55960966-T-C
gnomAD v3: 4-55094799-T-C
gnomAD v4: 4-55094799-T-C
MyVariant Identifiers: chr4:g.55960966T>C (hg19) chr4:g.55094799T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55094799T>C , CM000666.2:g.55094799T>C GRCh38
NC_000004.11:g.55960966T>C , CM000666.1:g.55960966T>C GRCh37
NC_000004.10:g.55655723T>C NCBI36
NG_012004.1:g.35797A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.2971+3A>G MANE Select ENSP00000263923.4:n.2971+3A>G
ENST00000647068.1:n.2984+3A>G
ENST00000263923.4:c.2971+3A>G ENSP00000263923.4:n.2971+3A>G
NM_002253.2:c.2971+3A>G NP_002244.1:n.2971+3A>G
NM_002253.3:c.2971+3A>G NP_002244.1:n.2971+3A>G
NM_002253.4:c.2971+3A>G MANE Select NP_002244.1:n.2971+3A>G
Search 100 bp 5'
Search 100 bp 3'