Canonical Allele Identifier: CA356913072
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs757898712
gnomAD v2: 4-55976680-A-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55110513A>C , CM000666.2:g.55110513A>C GRCh38
NC_000004.11:g.55976680A>C , CM000666.1:g.55976680A>C GRCh37
NC_000004.10:g.55671437A>C NCBI36
NG_012004.1:g.20083T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1145T>G MANE Select ENSP00000263923.4:p.Val382Gly
ENST00000647068.1:n.1158T>G
ENST00000263923.4:c.1145T>G ENSP00000263923.4:p.Val382Gly
ENST00000512566.1:n.1145T>G
NM_002253.2:c.1145T>G NP_002244.1:p.Val382Gly
NM_002253.3:c.1145T>G NP_002244.1:p.Val382Gly
NM_002253.4:c.1145T>G MANE Select NP_002244.1:p.Val382Gly