Canonical Allele Identifier: CA96891456
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1017656438
gnomAD v4: 4-55096573-C-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55096573C>A , CM000666.2:g.55096573C>A GRCh38
NC_000004.11:g.55962740C>A , CM000666.1:g.55962740C>A GRCh37
NC_000004.10:g.55657497C>A NCBI36
NG_012004.1:g.34023G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.2615-231G>T MANE Select ENSP00000263923.4:n.2615-231G>T
ENST00000647068.1:n.2628-231G>T
ENST00000263923.4:c.2615-231G>T ENSP00000263923.4:n.2615-231G>T
ENST00000509309.1:n.148G>T
NM_002253.2:c.2615-231G>T NP_002244.1:n.2615-231G>T
NM_002253.3:c.2615-231G>T NP_002244.1:n.2615-231G>T
NM_002253.4:c.2615-231G>T MANE Select NP_002244.1:n.2615-231G>T