Canonical Allele Identifier: CA356921317
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs2110039226

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125225A>T , CM000666.2:g.55125225A>T GRCh38
NC_000004.11:g.55991392A>T , CM000666.1:g.55991392A>T GRCh37
NC_000004.10:g.55686149A>T NCBI36
NG_012004.1:g.5371T>A

Transcript Alleles

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