Canonical Allele Identifier: CA1062710389
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1721013906
gnomAD v3: 4-55125559-A-C
gnomAD v4: 4-55125559-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125559A>C , CM000666.2:g.55125559A>C GRCh38
NC_000004.11:g.55991726A>C , CM000666.1:g.55991726A>C GRCh37
NC_000004.10:g.55686483A>C NCBI36
NG_012004.1:g.5037T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.-266T>G MANE Select ENSP00000263923.4:n.-266T>G
ENST00000263923.4:c.-266T>G ENSP00000263923.4:n.-266T>G
NM_002253.2:c.-266T>G NP_002244.1:n.-266T>G
NM_002253.3:c.-266T>G NP_002244.1:n.-266T>G
NM_002253.4:c.-266T>G MANE Select NP_002244.1:n.-266T>G