Canonical Allele Identifier: CA1062706322
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1720162910
gnomAD v3: 4-55096598-G-C
gnomAD v4: 4-55096598-G-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55096598G>C , CM000666.2:g.55096598G>C GRCh38
NC_000004.11:g.55962765G>C , CM000666.1:g.55962765G>C GRCh37
NC_000004.10:g.55657522G>C NCBI36
NG_012004.1:g.33998C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.2615-256C>G MANE Select ENSP00000263923.4:n.2615-256C>G
ENST00000647068.1:n.2628-256C>G
ENST00000263923.4:c.2615-256C>G ENSP00000263923.4:n.2615-256C>G
ENST00000509309.1:n.123C>G
NM_002253.2:c.2615-256C>G NP_002244.1:n.2615-256C>G
NM_002253.3:c.2615-256C>G NP_002244.1:n.2615-256C>G
NM_002253.4:c.2615-256C>G MANE Select NP_002244.1:n.2615-256C>G