Canonical Allele Identifier: CA1062704600
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1720016012
gnomAD v3: 4-55091442-C-A
gnomAD v4: 4-55091442-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091442C>A , CM000666.2:g.55091442C>A GRCh38
NC_000004.11:g.55957609C>A , CM000666.1:g.55957609C>A GRCh37
NC_000004.10:g.55652366C>A NCBI36
NG_012004.1:g.39154G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3069+1175G>T MANE Select ENSP00000263923.4:n.3069+1175G>T
ENST00000647068.1:n.3082+1175G>T
ENST00000263923.4:c.3069+1175G>T ENSP00000263923.4:n.3069+1175G>T
NM_002253.2:c.3069+1175G>T NP_002244.1:n.3069+1175G>T
NM_002253.3:c.3069+1175G>T NP_002244.1:n.3069+1175G>T
NM_002253.4:c.3069+1175G>T MANE Select NP_002244.1:n.3069+1175G>T