Canonical Allele Identifier: CA1458940101
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1578142799

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125190A>C , CM000666.2:g.55125190A>C GRCh38
NC_000004.11:g.55991357A>C , CM000666.1:g.55991357A>C GRCh37
NC_000004.10:g.55686114A>C NCBI36
NG_012004.1:g.5406T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.67+37T>G MANE Select ENSP00000263923.4:n.67+37T>G
ENST00000263923.4:c.67+37T>G ENSP00000263923.4:n.67+37T>G
ENST00000512566.1:n.67+37T>G
NM_002253.2:c.67+37T>G NP_002244.1:n.67+37T>G
NM_002253.3:c.67+37T>G NP_002244.1:n.67+37T>G
NM_002253.4:c.67+37T>G MANE Select NP_002244.1:n.67+37T>G