Canonical Allele Identifier: CA796419849
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1387802097

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091802T>C , CM000666.2:g.55091802T>C GRCh38
NC_000004.11:g.55957969T>C , CM000666.1:g.55957969T>C GRCh37
NC_000004.10:g.55652726T>C NCBI36
NG_012004.1:g.38794A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3069+815A>G MANE Select ENSP00000263923.4:n.3069+815A>G
ENST00000647068.1:n.3082+815A>G
ENST00000263923.4:c.3069+815A>G ENSP00000263923.4:n.3069+815A>G
NM_002253.2:c.3069+815A>G NP_002244.1:n.3069+815A>G
NM_002253.3:c.3069+815A>G NP_002244.1:n.3069+815A>G
NM_002253.4:c.3069+815A>G MANE Select NP_002244.1:n.3069+815A>G