Canonical Allele Identifier: CA96884013

Gene: KDR

Linked Data

• dbSNP Id: rs144155016
• gnomAD v2: 4-55957496-T-C
• gnomAD v3: 4-55091329-T-C
• gnomAD v4: 4-55091329-T-C
• MyVariant Identifiers: chr4:g.55957496T>C (hg19) ; chr4:g.55091329T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55091329T>C , CM000666.2:g.55091329T>C	GRCh38
NC_000004.11:g.55957496T>C , CM000666.1:g.55957496T>C	GRCh37
NC_000004.10:g.55652253T>C	NCBI36
NG_012004.1:g.39267A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263923.5:c.3070-1251A>G MANE Select	ENSP00000263923.4:n.3070-1251A>G
ENST00000647068.1:n.3083-1251A>G
ENST00000263923.4:c.3070-1251A>G	ENSP00000263923.4:n.3070-1251A>G
NM_002253.2:c.3070-1251A>G	NP_002244.1:n.3070-1251A>G
NM_002253.3:c.3070-1251A>G	NP_002244.1:n.3070-1251A>G
NM_002253.4:c.3070-1251A>G MANE Select	NP_002244.1:n.3070-1251A>G