Canonical Allele Identifier: CA2706106232
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs2110013036

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091815C>A , CM000666.2:g.55091815C>A GRCh38
NC_000004.11:g.55957982C>A , CM000666.1:g.55957982C>A GRCh37
NC_000004.10:g.55652739C>A NCBI36
NG_012004.1:g.38781G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3069+802G>T MANE Select ENSP00000263923.4:n.3069+802G>T
ENST00000647068.1:n.3082+802G>T
ENST00000263923.4:c.3069+802G>T ENSP00000263923.4:n.3069+802G>T
NM_002253.2:c.3069+802G>T NP_002244.1:n.3069+802G>T
NM_002253.3:c.3069+802G>T NP_002244.1:n.3069+802G>T
NM_002253.4:c.3069+802G>T MANE Select NP_002244.1:n.3069+802G>T