Canonical Allele Identifier: CA551377469

Gene: KDR

Linked Data

• dbSNP Id: rs1459563965
• gnomAD v2: 4-55957999-G-A
• gnomAD v3: 4-55091832-G-A
• gnomAD v4: 4-55091832-G-A
• MyVariant Identifiers: chr4:g.55957999G>A (hg19) ; chr4:g.55091832G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55091832G>A , CM000666.2:g.55091832G>A	GRCh38
NC_000004.11:g.55957999G>A , CM000666.1:g.55957999G>A	GRCh37
NC_000004.10:g.55652756G>A	NCBI36
NG_012004.1:g.38764C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263923.5:c.3069+785C>T MANE Select	ENSP00000263923.4:n.3069+785C>T
ENST00000647068.1:n.3082+785C>T
ENST00000263923.4:c.3069+785C>T	ENSP00000263923.4:n.3069+785C>T
NM_002253.2:c.3069+785C>T	NP_002244.1:n.3069+785C>T
NM_002253.3:c.3069+785C>T	NP_002244.1:n.3069+785C>T
NM_002253.4:c.3069+785C>T MANE Select	NP_002244.1:n.3069+785C>T