Canonical Allele Identifier: CA96921198

Gene: KDR

Linked Data

• dbSNP Id: rs569504730
• gnomAD v2: 4-55991091-C-T
• gnomAD v3: 4-55124924-C-T
• gnomAD v4: 4-55124924-C-T
• MyVariant Identifiers: chr4:g.55991091C>T (hg19) ; chr4:g.55124924C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55124924C>T , CM000666.2:g.55124924C>T	GRCh38
NC_000004.11:g.55991091C>T , CM000666.1:g.55991091C>T	GRCh37
NC_000004.10:g.55685848C>T	NCBI36
NG_012004.1:g.5672G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263923.5:c.67+303G>A MANE Select	ENSP00000263923.4:n.67+303G>A
ENST00000263923.4:c.67+303G>A	ENSP00000263923.4:n.67+303G>A
ENST00000512566.1:n.67+303G>A
NM_002253.2:c.67+303G>A	NP_002244.1:n.67+303G>A
NM_002253.3:c.67+303G>A	NP_002244.1:n.67+303G>A
NM_002253.4:c.67+303G>A MANE Select	NP_002244.1:n.67+303G>A