Canonical Allele Identifier: CA551382515
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1364502029
gnomAD v2: 4-55991484-T-A
MyVariant Identifiers: chr4:g.55991484T>A (hg19) chr4:g.55125317T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125317T>A , CM000666.2:g.55125317T>A GRCh38
NC_000004.11:g.55991484T>A , CM000666.1:g.55991484T>A GRCh37
NC_000004.10:g.55686241T>A NCBI36
NG_012004.1:g.5279A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.-24A>T MANE Select ENSP00000263923.4:n.-24A>T
ENST00000263923.4:c.-24A>T ENSP00000263923.4:n.-24A>T
NM_002253.2:c.-24A>T NP_002244.1:n.-24A>T
NM_002253.3:c.-24A>T NP_002244.1:n.-24A>T
NM_002253.4:c.-24A>T MANE Select NP_002244.1:n.-24A>T
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