Canonical Allele Identifier: CA96921562
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1007267693
gnomAD v2: 4-55991369-T-G
gnomAD v3: 4-55125202-T-G
gnomAD v4: 4-55125202-T-G
MyVariant Identifiers: chr4:g.55991369T>G (hg19) chr4:g.55125202T>G (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125202T>G , CM000666.2:g.55125202T>G GRCh38
NC_000004.11:g.55991369T>G , CM000666.1:g.55991369T>G GRCh37
NC_000004.10:g.55686126T>G NCBI36
NG_012004.1:g.5394A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.67+25A>C MANE Select ENSP00000263923.4:n.67+25A>C
ENST00000263923.4:c.67+25A>C ENSP00000263923.4:n.67+25A>C
ENST00000512566.1:n.67+25A>C
NM_002253.2:c.67+25A>C NP_002244.1:n.67+25A>C
NM_002253.3:c.67+25A>C NP_002244.1:n.67+25A>C
NM_002253.4:c.67+25A>C MANE Select NP_002244.1:n.67+25A>C
Search 100 bp 5'
Search 100 bp 3'