Canonical Allele Identifier: CA356913461
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1302908825
gnomAD v2: 4-55976864-T-G
MyVariant Identifiers: chr4:g.55976864T>G (hg19) chr4:g.55110697T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55110697T>G , CM000666.2:g.55110697T>G GRCh38
NC_000004.11:g.55976864T>G , CM000666.1:g.55976864T>G GRCh37
NC_000004.10:g.55671621T>G NCBI36
NG_012004.1:g.19899A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1048A>C MANE Select ENSP00000263923.4:p.Ile350Leu
ENST00000647068.1:n.1061A>C
ENST00000263923.4:c.1048A>C ENSP00000263923.4:p.Ile350Leu
ENST00000512566.1:n.1048A>C
NM_002253.2:c.1048A>C NP_002244.1:p.Ile350Leu
NM_002253.3:c.1048A>C NP_002244.1:p.Ile350Leu
NM_002253.4:c.1048A>C MANE Select NP_002244.1:p.Ile350Leu
Search 100 bp 5'
Search 100 bp 3'