Canonical Allele Identifier: CA356913027
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs2110027441
MyVariant Identifiers: chr4:g.55976666C>G (hg19) chr4:g.55110499C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55110499C>G , CM000666.2:g.55110499C>G GRCh38
NC_000004.11:g.55976666C>G , CM000666.1:g.55976666C>G GRCh37
NC_000004.10:g.55671423C>G NCBI36
NG_012004.1:g.20097G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1159G>C MANE Select ENSP00000263923.4:p.Glu387Gln
ENST00000647068.1:n.1172G>C
ENST00000263923.4:c.1159G>C ENSP00000263923.4:p.Glu387Gln
ENST00000512566.1:n.1159G>C
NM_002253.2:c.1159G>C NP_002244.1:p.Glu387Gln
NM_002253.3:c.1159G>C NP_002244.1:p.Glu387Gln
NM_002253.4:c.1159G>C MANE Select NP_002244.1:p.Glu387Gln
Search 100 bp 5'
Search 100 bp 3'