Canonical Allele Identifier: CA439631993
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs2110027487
gnomAD v4: 4-55110512-T-A
MyVariant Identifiers: chr4:g.55976679T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55110512T>A , CM000666.2:g.55110512T>A GRCh38
NC_000004.11:g.55976679T>A , CM000666.1:g.55976679T>A GRCh37
NC_000004.10:g.55671436T>A NCBI36
NG_012004.1:g.20084A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1146A>T MANE Select ENSP00000263923.4:p.Val382=
ENST00000647068.1:n.1159A>T
ENST00000263923.4:c.1146A>T ENSP00000263923.4:p.Val382=
ENST00000512566.1:n.1146A>T
NM_002253.2:c.1146A>T NP_002244.1:p.Val382=
NM_002253.3:c.1146A>T NP_002244.1:p.Val382=
NM_002253.4:c.1146A>T MANE Select NP_002244.1:p.Val382=