Canonical Allele Identifier: CA2706106549
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs2110027742

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55110599T>C , CM000666.2:g.55110599T>C GRCh38
NC_000004.11:g.55976766T>C , CM000666.1:g.55976766T>C GRCh37
NC_000004.10:g.55671523T>C NCBI36
NG_012004.1:g.19997A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1092-33A>G MANE Select ENSP00000263923.4:n.1092-33A>G
ENST00000647068.1:n.1105-33A>G
ENST00000263923.4:c.1092-33A>G ENSP00000263923.4:n.1092-33A>G
ENST00000512566.1:n.1092-33A>G
NM_002253.2:c.1092-33A>G NP_002244.1:n.1092-33A>G
NM_002253.3:c.1092-33A>G NP_002244.1:n.1092-33A>G
NM_002253.4:c.1092-33A>G MANE Select NP_002244.1:n.1092-33A>G