Canonical Allele Identifier: CA356913056
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs201708587
MyVariant Identifiers: chr4:g.55976674G>C (hg19) chr4:g.55110507G>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55110507G>C , CM000666.2:g.55110507G>C GRCh38
NC_000004.11:g.55976674G>C , CM000666.1:g.55976674G>C GRCh37
NC_000004.10:g.55671431G>C NCBI36
NG_012004.1:g.20089C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1151C>G MANE Select ENSP00000263923.4:p.Thr384Arg
ENST00000647068.1:n.1164C>G
ENST00000263923.4:c.1151C>G ENSP00000263923.4:p.Thr384Arg
ENST00000512566.1:n.1151C>G
NM_002253.2:c.1151C>G NP_002244.1:p.Thr384Arg
NM_002253.3:c.1151C>G NP_002244.1:p.Thr384Arg
NM_002253.4:c.1151C>G MANE Select NP_002244.1:p.Thr384Arg
Search 100 bp 5'
Search 100 bp 3'