Canonical Allele Identifier: CA96884238

Gene: KDR

Linked Data

• dbSNP Id: rs988658869
• gnomAD v2: 4-55957780-A-G
• gnomAD v3: 4-55091613-A-G
• gnomAD v4: 4-55091613-A-G
• MyVariant Identifiers: chr4:g.55957780A>G (hg19) ; chr4:g.55091613A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55091613A>G , CM000666.2:g.55091613A>G	GRCh38
NC_000004.11:g.55957780A>G , CM000666.1:g.55957780A>G	GRCh37
NC_000004.10:g.55652537A>G	NCBI36
NG_012004.1:g.38983T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263923.5:c.3069+1004T>C MANE Select	ENSP00000263923.4:n.3069+1004T>C
ENST00000647068.1:n.3082+1004T>C
ENST00000263923.4:c.3069+1004T>C	ENSP00000263923.4:n.3069+1004T>C
NM_002253.2:c.3069+1004T>C	NP_002244.1:n.3069+1004T>C
NM_002253.3:c.3069+1004T>C	NP_002244.1:n.3069+1004T>C
NM_002253.4:c.3069+1004T>C MANE Select	NP_002244.1:n.3069+1004T>C