Canonical Allele Identifier: CA96908161
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1054196581
gnomAD v2: 4-55978884-A-G
gnomAD v3: 4-55112717-A-G
gnomAD v4: 4-55112717-A-G
MyVariant Identifiers: chr4:g.55978884A>G (hg19) chr4:g.55112717A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55112717A>G , CM000666.2:g.55112717A>G GRCh38
NC_000004.11:g.55978884A>G , CM000666.1:g.55978884A>G GRCh37
NC_000004.10:g.55673641A>G NCBI36
NG_012004.1:g.17879T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.976+587T>C MANE Select ENSP00000263923.4:n.976+587T>C
ENST00000647068.1:n.989+587T>C
ENST00000263923.4:c.976+587T>C ENSP00000263923.4:n.976+587T>C
ENST00000512566.1:n.976+587T>C
NM_002253.2:c.976+587T>C NP_002244.1:n.976+587T>C
NM_002253.3:c.976+587T>C NP_002244.1:n.976+587T>C
NM_002253.4:c.976+587T>C MANE Select NP_002244.1:n.976+587T>C
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