Canonical Allele Identifier: CA96922075
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs113321180
gnomAD v2: 4-55991672-A-G
gnomAD v3: 4-55125505-A-G
gnomAD v4: 4-55125505-A-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125505A>G , CM000666.2:g.55125505A>G GRCh38
NC_000004.11:g.55991672A>G , CM000666.1:g.55991672A>G GRCh37
NC_000004.10:g.55686429A>G NCBI36
NG_012004.1:g.5091T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.-212T>C MANE Select ENSP00000263923.4:n.-212T>C
ENST00000263923.4:c.-212T>C ENSP00000263923.4:n.-212T>C
NM_002253.2:c.-212T>C NP_002244.1:n.-212T>C
NM_002253.3:c.-212T>C NP_002244.1:n.-212T>C
NM_002253.4:c.-212T>C MANE Select NP_002244.1:n.-212T>C