Canonical Allele Identifier: CA356921323
Gene: KDR HGNC NCBI

Linked Data

MyVariant Identifiers: chr4:g.55991393C>G (hg19) chr4:g.55125226C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125226C>G , CM000666.2:g.55125226C>G GRCh38
NC_000004.11:g.55991393C>G , CM000666.1:g.55991393C>G GRCh37
NC_000004.10:g.55686150C>G NCBI36
NG_012004.1:g.5370G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.67+1G>C MANE Select ENSP00000263923.4:n.67+1G>C
ENST00000263923.4:c.67+1G>C ENSP00000263923.4:n.67+1G>C
ENST00000512566.1:n.67+1G>C
NM_002253.2:c.67+1G>C NP_002244.1:n.67+1G>C
NM_002253.3:c.67+1G>C NP_002244.1:n.67+1G>C
NM_002253.4:c.67+1G>C MANE Select NP_002244.1:n.67+1G>C
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