Canonical Allele Identifier: CA551377394
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1248411164
gnomAD v2: 4-55957863-C-A
gnomAD v3: 4-55091696-C-A
gnomAD v4: 4-55091696-C-A
MyVariant Identifiers: chr4:g.55957863C>A (hg19) chr4:g.55957863_55957864delinsAA (hg19) chr4:g.55091696C>A (hg38) chr4:g.55091696_55091697delinsAA (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091696C>A , CM000666.2:g.55091696C>A GRCh38
NC_000004.11:g.55957863C>A , CM000666.1:g.55957863C>A GRCh37
NC_000004.10:g.55652620C>A NCBI36
NG_012004.1:g.38900G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3069+921G>T MANE Select ENSP00000263923.4:n.3069+921G>T
ENST00000647068.1:n.3082+921G>T
ENST00000263923.4:c.3069+921G>T ENSP00000263923.4:n.3069+921G>T
NM_002253.2:c.3069+921G>T NP_002244.1:n.3069+921G>T
NM_002253.3:c.3069+921G>T NP_002244.1:n.3069+921G>T
NM_002253.4:c.3069+921G>T MANE Select NP_002244.1:n.3069+921G>T
Search 100 bp 5'
Search 100 bp 3'