Canonical Allele Identifier: CA356913063
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs2110027475
MyVariant Identifiers: chr4:g.55976675T>C (hg19) chr4:g.55110508T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55110508T>C , CM000666.2:g.55110508T>C GRCh38
NC_000004.11:g.55976675T>C , CM000666.1:g.55976675T>C GRCh37
NC_000004.10:g.55671432T>C NCBI36
NG_012004.1:g.20088A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1150A>G MANE Select ENSP00000263923.4:p.Thr384Ala
ENST00000647068.1:n.1163A>G
ENST00000263923.4:c.1150A>G ENSP00000263923.4:p.Thr384Ala
ENST00000512566.1:n.1150A>G
NM_002253.2:c.1150A>G NP_002244.1:p.Thr384Ala
NM_002253.3:c.1150A>G NP_002244.1:p.Thr384Ala
NM_002253.4:c.1150A>G MANE Select NP_002244.1:p.Thr384Ala
Search 100 bp 5'
Search 100 bp 3'