Canonical Allele Identifier: CA796407492
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1354736431
gnomAD v3: 4-55125506-C-T
gnomAD v4: 4-55125506-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125506C>T , CM000666.2:g.55125506C>T GRCh38
NC_000004.11:g.55991673C>T , CM000666.1:g.55991673C>T GRCh37
NC_000004.10:g.55686430C>T NCBI36
NG_012004.1:g.5090G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.-213G>A MANE Select ENSP00000263923.4:n.-213G>A
ENST00000263923.4:c.-213G>A ENSP00000263923.4:n.-213G>A
NM_002253.2:c.-213G>A NP_002244.1:n.-213G>A
NM_002253.3:c.-213G>A NP_002244.1:n.-213G>A
NM_002253.4:c.-213G>A MANE Select NP_002244.1:n.-213G>A