Canonical Allele Identifier: CA1458933482
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1578138056

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55112625T>G , CM000666.2:g.55112625T>G GRCh38
NC_000004.11:g.55978792T>G , CM000666.1:g.55978792T>G GRCh37
NC_000004.10:g.55673549T>G NCBI36
NG_012004.1:g.17971A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.976+679A>C MANE Select ENSP00000263923.4:n.976+679A>C
ENST00000647068.1:n.989+679A>C
ENST00000263923.4:c.976+679A>C ENSP00000263923.4:n.976+679A>C
ENST00000512566.1:n.976+679A>C
NM_002253.2:c.976+679A>C NP_002244.1:n.976+679A>C
NM_002253.3:c.976+679A>C NP_002244.1:n.976+679A>C
NM_002253.4:c.976+679A>C MANE Select NP_002244.1:n.976+679A>C