Canonical Allele Identifier: CA96891447
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1018261238
MyVariant Identifiers: chr4:g.55962726A>G (hg19) chr4:g.55096559A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55096559A>G , CM000666.2:g.55096559A>G GRCh38
NC_000004.11:g.55962726A>G , CM000666.1:g.55962726A>G GRCh37
NC_000004.10:g.55657483A>G NCBI36
NG_012004.1:g.34037T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.2615-217T>C MANE Select ENSP00000263923.4:n.2615-217T>C
ENST00000647068.1:n.2628-217T>C
ENST00000263923.4:c.2615-217T>C ENSP00000263923.4:n.2615-217T>C
ENST00000509309.1:n.162T>C
NM_002253.2:c.2615-217T>C NP_002244.1:n.2615-217T>C
NM_002253.3:c.2615-217T>C NP_002244.1:n.2615-217T>C
NM_002253.4:c.2615-217T>C MANE Select NP_002244.1:n.2615-217T>C
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