Canonical Allele Identifier: CA96921273
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs948632667

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55124965A>G , CM000666.2:g.55124965A>G GRCh38
NC_000004.11:g.55991132A>G , CM000666.1:g.55991132A>G GRCh37
NC_000004.10:g.55685889A>G NCBI36
NG_012004.1:g.5631T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.67+262T>C MANE Select ENSP00000263923.4:n.67+262T>C
ENST00000263923.4:c.67+262T>C ENSP00000263923.4:n.67+262T>C
ENST00000512566.1:n.67+262T>C
NM_002253.2:c.67+262T>C NP_002244.1:n.67+262T>C
NM_002253.3:c.67+262T>C NP_002244.1:n.67+262T>C
NM_002253.4:c.67+262T>C MANE Select NP_002244.1:n.67+262T>C