Canonical Allele Identifier: CA96921197
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1056627388
gnomAD v2: 4-55991084-G-C
gnomAD v3: 4-55124917-G-C
gnomAD v4: 4-55124917-G-C
MyVariant Identifiers: chr4:g.55991084G>C (hg19) chr4:g.55124917G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55124917G>C , CM000666.2:g.55124917G>C GRCh38
NC_000004.11:g.55991084G>C , CM000666.1:g.55991084G>C GRCh37
NC_000004.10:g.55685841G>C NCBI36
NG_012004.1:g.5679C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.67+310C>G MANE Select ENSP00000263923.4:n.67+310C>G
ENST00000263923.4:c.67+310C>G ENSP00000263923.4:n.67+310C>G
ENST00000512566.1:n.67+310C>G
NM_002253.2:c.67+310C>G NP_002244.1:n.67+310C>G
NM_002253.3:c.67+310C>G NP_002244.1:n.67+310C>G
NM_002253.4:c.67+310C>G MANE Select NP_002244.1:n.67+310C>G
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