Canonical Allele Identifier: CA796419877
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1371208706
gnomAD v3: 4-55091885-A-T
gnomAD v4: 4-55091885-A-T
MyVariant Identifiers: chr4:g.55958052A>T (hg19) chr4:g.55091885A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091885A>T , CM000666.2:g.55091885A>T GRCh38
NC_000004.11:g.55958052A>T , CM000666.1:g.55958052A>T GRCh37
NC_000004.10:g.55652809A>T NCBI36
NG_012004.1:g.38711T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3069+732T>A MANE Select ENSP00000263923.4:n.3069+732T>A
ENST00000647068.1:n.3082+732T>A
ENST00000263923.4:c.3069+732T>A ENSP00000263923.4:n.3069+732T>A
NM_002253.2:c.3069+732T>A NP_002244.1:n.3069+732T>A
NM_002253.3:c.3069+732T>A NP_002244.1:n.3069+732T>A
NM_002253.4:c.3069+732T>A MANE Select NP_002244.1:n.3069+732T>A
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