Canonical Allele Identifier: CA551382478
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs751347443
gnomAD v2: 4-55991368-T-C
gnomAD v4: 4-55125201-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125201T>C , CM000666.2:g.55125201T>C GRCh38
NC_000004.11:g.55991368T>C , CM000666.1:g.55991368T>C GRCh37
NC_000004.10:g.55686125T>C NCBI36
NG_012004.1:g.5395A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263923.5:c.67+26A>G MANE Select ENSP00000263923.4:n.67+26A>G
ENST00000263923.4:c.67+26A>G ENSP00000263923.4:n.67+26A>G
ENST00000512566.1:n.67+26A>G
NM_002253.2:c.67+26A>G NP_002244.1:n.67+26A>G
NM_002253.3:c.67+26A>G NP_002244.1:n.67+26A>G
NM_002253.4:c.67+26A>G MANE Select NP_002244.1:n.67+26A>G