Canonical Allele Identifier: CA96921579
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1038659265
gnomAD v4: 4-55125213-A-G
MyVariant Identifiers: chr4:g.55125213A>G (hg38)

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125213A>G , CM000666.2:g.55125213A>G GRCh38
NC_000004.11:g.55991380A>G , CM000666.1:g.55991380A>G GRCh37
NC_000004.10:g.55686137A>G NCBI36
NG_012004.1:g.5383T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263923.5:c.67+14T>C MANE Select ENSP00000263923.4:n.67+14T>C
ENST00000263923.4:c.67+14T>C ENSP00000263923.4:n.67+14T>C
ENST00000512566.1:n.67+14T>C
NM_002253.2:c.67+14T>C NP_002244.1:n.67+14T>C
NM_002253.3:c.67+14T>C NP_002244.1:n.67+14T>C
NM_002253.4:c.67+14T>C MANE Select NP_002244.1:n.67+14T>C