Canonical Allele Identifier: CA96908201
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs910042781
MyVariant Identifiers: chr4:g.55978925G>C (hg19) chr4:g.55112758G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55112758G>C , CM000666.2:g.55112758G>C GRCh38
NC_000004.11:g.55978925G>C , CM000666.1:g.55978925G>C GRCh37
NC_000004.10:g.55673682G>C NCBI36
NG_012004.1:g.17838C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263923.5:c.976+546C>G MANE Select ENSP00000263923.4:n.976+546C>G
ENST00000647068.1:n.989+546C>G
ENST00000263923.4:c.976+546C>G ENSP00000263923.4:n.976+546C>G
ENST00000512566.1:n.976+546C>G
NM_002253.2:c.976+546C>G NP_002244.1:n.976+546C>G
NM_002253.3:c.976+546C>G NP_002244.1:n.976+546C>G
NM_002253.4:c.976+546C>G MANE Select NP_002244.1:n.976+546C>G
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