Canonical Allele Identifier: CA96921886

Gene: KDR

Linked Data

• dbSNP Id: rs919430835
• gnomAD v3: 4-55125402-G-T
• gnomAD v4: 4-55125402-G-T
• MyVariant Identifiers: chr4:g.55991569G>T (hg19) ; chr4:g.55125402G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55125402G>T , CM000666.2:g.55125402G>T	GRCh38
NC_000004.11:g.55991569G>T , CM000666.1:g.55991569G>T	GRCh37
NC_000004.10:g.55686326G>T	NCBI36
NG_012004.1:g.5194C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263923.5:c.-109C>A MANE Select	ENSP00000263923.4:n.-109C>A
ENST00000263923.4:c.-109C>A	ENSP00000263923.4:n.-109C>A
NM_002253.2:c.-109C>A	NP_002244.1:n.-109C>A
NM_002253.3:c.-109C>A	NP_002244.1:n.-109C>A
NM_002253.4:c.-109C>A MANE Select	NP_002244.1:n.-109C>A