Canonical Allele Identifier: CA96922005
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs896357396
gnomAD v3: 4-55125449-G-A
gnomAD v4: 4-55125449-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125449G>A , CM000666.2:g.55125449G>A GRCh38
NC_000004.11:g.55991616G>A , CM000666.1:g.55991616G>A GRCh37
NC_000004.10:g.55686373G>A NCBI36
NG_012004.1:g.5147C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.-156C>T MANE Select ENSP00000263923.4:n.-156C>T
ENST00000263923.4:c.-156C>T ENSP00000263923.4:n.-156C>T
NM_002253.2:c.-156C>T NP_002244.1:n.-156C>T
NM_002253.3:c.-156C>T NP_002244.1:n.-156C>T
NM_002253.4:c.-156C>T MANE Select NP_002244.1:n.-156C>T