Canonical Allele Identifier: CA551381365
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1319545108
gnomAD v2: 4-55979010-T-G
gnomAD v3: 4-55112843-T-G
gnomAD v4: 4-55112843-T-G
MyVariant Identifiers: chr4:g.55979010T>G (hg19) chr4:g.55112843T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55112843T>G , CM000666.2:g.55112843T>G GRCh38
NC_000004.11:g.55979010T>G , CM000666.1:g.55979010T>G GRCh37
NC_000004.10:g.55673767T>G NCBI36
NG_012004.1:g.17753A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263923.5:c.976+461A>C MANE Select ENSP00000263923.4:n.976+461A>C
ENST00000647068.1:n.989+461A>C
ENST00000263923.4:c.976+461A>C ENSP00000263923.4:n.976+461A>C
ENST00000512566.1:n.976+461A>C
NM_002253.2:c.976+461A>C NP_002244.1:n.976+461A>C
NM_002253.3:c.976+461A>C NP_002244.1:n.976+461A>C
NM_002253.4:c.976+461A>C MANE Select NP_002244.1:n.976+461A>C
Search 100 bp 5'
Search 100 bp 3'