Canonical Allele Identifier: CA96884085

Gene: KDR

Linked Data

• dbSNP Id: rs543555111
• gnomAD v3: 4-55091458-A-G
• gnomAD v4: 4-55091458-A-G
• MyVariant Identifiers: chr4:g.55957625A>G (hg19) ; chr4:g.55091458A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55091458A>G , CM000666.2:g.55091458A>G	GRCh38
NC_000004.11:g.55957625A>G , CM000666.1:g.55957625A>G	GRCh37
NC_000004.10:g.55652382A>G	NCBI36
NG_012004.1:g.39138T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000263923.5:c.3069+1159T>C MANE Select	ENSP00000263923.4:n.3069+1159T>C
ENST00000647068.1:n.3082+1159T>C
ENST00000263923.4:c.3069+1159T>C	ENSP00000263923.4:n.3069+1159T>C
NM_002253.2:c.3069+1159T>C	NP_002244.1:n.3069+1159T>C
NM_002253.3:c.3069+1159T>C	NP_002244.1:n.3069+1159T>C
NM_002253.4:c.3069+1159T>C MANE Select	NP_002244.1:n.3069+1159T>C