Canonical Allele Identifier: CA96922066

Gene: KDR

Linked Data

• dbSNP Id: rs552965525
• gnomAD v2: 4-55991656-C-A
• gnomAD v3: 4-55125489-C-A
• gnomAD v4: 4-55125489-C-A
• MyVariant Identifiers: chr4:g.55991656C>A (hg19) ; chr4:g.55125489C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55125489C>A , CM000666.2:g.55125489C>A	GRCh38
NC_000004.11:g.55991656C>A , CM000666.1:g.55991656C>A	GRCh37
NC_000004.10:g.55686413C>A	NCBI36
NG_012004.1:g.5107G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263923.5:c.-196G>T MANE Select	ENSP00000263923.4:n.-196G>T
ENST00000263923.4:c.-196G>T	ENSP00000263923.4:n.-196G>T
NM_002253.2:c.-196G>T	NP_002244.1:n.-196G>T
NM_002253.3:c.-196G>T	NP_002244.1:n.-196G>T
NM_002253.4:c.-196G>T MANE Select	NP_002244.1:n.-196G>T