Canonical Allele Identifier: CA356913065
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs2110027480
MyVariant Identifiers: chr4:g.55976677A>G (hg19) chr4:g.55110510A>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55110510A>G , CM000666.2:g.55110510A>G GRCh38
NC_000004.11:g.55976677A>G , CM000666.1:g.55976677A>G GRCh37
NC_000004.10:g.55671434A>G NCBI36
NG_012004.1:g.20086T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1148T>C MANE Select ENSP00000263923.4:p.Leu383Pro
ENST00000647068.1:n.1161T>C
ENST00000263923.4:c.1148T>C ENSP00000263923.4:p.Leu383Pro
ENST00000512566.1:n.1148T>C
NM_002253.2:c.1148T>C NP_002244.1:p.Leu383Pro
NM_002253.3:c.1148T>C NP_002244.1:p.Leu383Pro
NM_002253.4:c.1148T>C MANE Select NP_002244.1:p.Leu383Pro
Search 100 bp 5'
Search 100 bp 3'