Canonical Allele Identifier: CA96908211
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs907165261
MyVariant Identifiers: chr4:g.55112778C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55112778C>A , CM000666.2:g.55112778C>A GRCh38
NC_000004.11:g.55978945C>A , CM000666.1:g.55978945C>A GRCh37
NC_000004.10:g.55673702C>A NCBI36
NG_012004.1:g.17818G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000263923.5:c.976+526G>T MANE Select ENSP00000263923.4:n.976+526G>T
ENST00000647068.1:n.989+526G>T
ENST00000263923.4:c.976+526G>T ENSP00000263923.4:n.976+526G>T
ENST00000512566.1:n.976+526G>T
NM_002253.2:c.976+526G>T NP_002244.1:n.976+526G>T
NM_002253.3:c.976+526G>T NP_002244.1:n.976+526G>T
NM_002253.4:c.976+526G>T MANE Select NP_002244.1:n.976+526G>T
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