Canonical Allele Identifier: CA551651743
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1419285011
gnomAD v2: 4-55976751-C-T
gnomAD v4: 4-55110584-C-T
MyVariant Identifiers: chr4:g.55976751C>T (hg19) chr4:g.55110584C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55110584C>T , CM000666.2:g.55110584C>T GRCh38
NC_000004.11:g.55976751C>T , CM000666.1:g.55976751C>T GRCh37
NC_000004.10:g.55671508C>T NCBI36
NG_012004.1:g.20012G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1092-18G>A MANE Select ENSP00000263923.4:n.1092-18G>A
ENST00000647068.1:n.1105-18G>A
ENST00000263923.4:c.1092-18G>A ENSP00000263923.4:n.1092-18G>A
ENST00000512566.1:n.1092-18G>A
NM_002253.2:c.1092-18G>A NP_002244.1:n.1092-18G>A
NM_002253.3:c.1092-18G>A NP_002244.1:n.1092-18G>A
NM_002253.4:c.1092-18G>A MANE Select NP_002244.1:n.1092-18G>A
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