Canonical Allele Identifier: CA551382519
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs114484350
gnomAD v2: 4-55991510-T-G
gnomAD v4: 4-55125343-T-G
MyVariant Identifiers: chr4:g.55991510T>G (hg19) chr4:g.55125343T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125343T>G , CM000666.2:g.55125343T>G GRCh38
NC_000004.11:g.55991510T>G , CM000666.1:g.55991510T>G GRCh37
NC_000004.10:g.55686267T>G NCBI36
NG_012004.1:g.5253A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.-50A>C MANE Select ENSP00000263923.4:n.-50A>C
ENST00000263923.4:c.-50A>C ENSP00000263923.4:n.-50A>C
NM_002253.2:c.-50A>C NP_002244.1:n.-50A>C
NM_002253.3:c.-50A>C NP_002244.1:n.-50A>C
NM_002253.4:c.-50A>C MANE Select NP_002244.1:n.-50A>C
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