Canonical Allele Identifier: CA96908264

Gene: KDR

Linked Data

• dbSNP Id: rs181505016
• gnomAD v2: 4-55978986-C-T
• gnomAD v3: 4-55112819-C-T
• gnomAD v4: 4-55112819-C-T
• MyVariant Identifiers: chr4:g.55978986C>T (hg19) ; chr4:g.55112819C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55112819C>T , CM000666.2:g.55112819C>T	GRCh38
NC_000004.11:g.55978986C>T , CM000666.1:g.55978986C>T	GRCh37
NC_000004.10:g.55673743C>T	NCBI36
NG_012004.1:g.17777G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000263923.5:c.976+485G>A MANE Select	ENSP00000263923.4:n.976+485G>A
ENST00000647068.1:n.989+485G>A
ENST00000263923.4:c.976+485G>A	ENSP00000263923.4:n.976+485G>A
ENST00000512566.1:n.976+485G>A
NM_002253.2:c.976+485G>A	NP_002244.1:n.976+485G>A
NM_002253.3:c.976+485G>A	NP_002244.1:n.976+485G>A
NM_002253.4:c.976+485G>A MANE Select	NP_002244.1:n.976+485G>A