Canonical Allele Identifier: CA356913274

Gene: KDR

Linked Data

• dbSNP Id: rs2110027660
• MyVariant Identifiers: chr4:g.55976734C>G (hg19) ; chr4:g.55110567C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55110567C>G , CM000666.2:g.55110567C>G	GRCh38
NC_000004.11:g.55976734C>G , CM000666.1:g.55976734C>G	GRCh37
NC_000004.10:g.55671491C>G	NCBI36
NG_012004.1:g.20029G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263923.5:c.1092-1G>C MANE Select	ENSP00000263923.4:n.1092-1G>C
ENST00000647068.1:n.1105-1G>C
ENST00000263923.4:c.1092-1G>C	ENSP00000263923.4:n.1092-1G>C
ENST00000512566.1:n.1092-1G>C
NM_002253.2:c.1092-1G>C	NP_002244.1:n.1092-1G>C
NM_002253.3:c.1092-1G>C	NP_002244.1:n.1092-1G>C
NM_002253.4:c.1092-1G>C MANE Select	NP_002244.1:n.1092-1G>C