Canonical Allele Identifier: CA1062704595
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1720015943
gnomAD v3: 4-55091441-T-A
gnomAD v4: 4-55091441-T-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091441T>A , CM000666.2:g.55091441T>A GRCh38
NC_000004.11:g.55957608T>A , CM000666.1:g.55957608T>A GRCh37
NC_000004.10:g.55652365T>A NCBI36
NG_012004.1:g.39155A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3069+1176A>T MANE Select ENSP00000263923.4:n.3069+1176A>T
ENST00000647068.1:n.3082+1176A>T
ENST00000263923.4:c.3069+1176A>T ENSP00000263923.4:n.3069+1176A>T
NM_002253.2:c.3069+1176A>T NP_002244.1:n.3069+1176A>T
NM_002253.3:c.3069+1176A>T NP_002244.1:n.3069+1176A>T
NM_002253.4:c.3069+1176A>T MANE Select NP_002244.1:n.3069+1176A>T