Canonical Allele Identifier: CA1458926490
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1040828041

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55087315C>G , CM000666.2:g.55087315C>G GRCh38
NC_000004.11:g.55953482C>G , CM000666.1:g.55953482C>G GRCh37
NC_000004.10:g.55648239C>G NCBI36
NG_012004.1:g.43281G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000263923.5:c.3662+292G>C MANE Select ENSP00000263923.4:n.3662+292G>C
ENST00000647068.1:n.3675+292G>C
ENST00000263923.4:c.3662+292G>C ENSP00000263923.4:n.3662+292G>C
NM_002253.2:c.3662+292G>C NP_002244.1:n.3662+292G>C
NM_002253.3:c.3662+292G>C NP_002244.1:n.3662+292G>C
NM_002253.4:c.3662+292G>C MANE Select NP_002244.1:n.3662+292G>C