Canonical Allele Identifier: CA796406958
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1261027789
gnomAD v3: 4-55124903-T-G
gnomAD v4: 4-55124903-T-G
MyVariant Identifiers: chr4:g.55991070T>G (hg19) chr4:g.55124903T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55124903T>G , CM000666.2:g.55124903T>G GRCh38
NC_000004.11:g.55991070T>G , CM000666.1:g.55991070T>G GRCh37
NC_000004.10:g.55685827T>G NCBI36
NG_012004.1:g.5693A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.67+324A>C MANE Select ENSP00000263923.4:n.67+324A>C
ENST00000263923.4:c.67+324A>C ENSP00000263923.4:n.67+324A>C
ENST00000512566.1:n.67+324A>C
NM_002253.2:c.67+324A>C NP_002244.1:n.67+324A>C
NM_002253.3:c.67+324A>C NP_002244.1:n.67+324A>C
NM_002253.4:c.67+324A>C MANE Select NP_002244.1:n.67+324A>C
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