Canonical Allele Identifier: CA356913105
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs747477930
MyVariant Identifiers: chr4:g.55976689G>C (hg19) chr4:g.55110522G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55110522G>C , CM000666.2:g.55110522G>C GRCh38
NC_000004.11:g.55976689G>C , CM000666.1:g.55976689G>C GRCh37
NC_000004.10:g.55671446G>C NCBI36
NG_012004.1:g.20074C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1136C>G MANE Select ENSP00000263923.4:p.Ala379Gly
ENST00000647068.1:n.1149C>G
ENST00000263923.4:c.1136C>G ENSP00000263923.4:p.Ala379Gly
ENST00000512566.1:n.1136C>G
NM_002253.2:c.1136C>G NP_002244.1:p.Ala379Gly
NM_002253.3:c.1136C>G NP_002244.1:p.Ala379Gly
NM_002253.4:c.1136C>G MANE Select NP_002244.1:p.Ala379Gly
Search 100 bp 5'
Search 100 bp 3'