Canonical Allele Identifier: CA796407329
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1311011150
gnomAD v4: 4-55125325-A-T
MyVariant Identifiers: chr4:g.55991492A>T (hg19) chr4:g.55125325A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125325A>T , CM000666.2:g.55125325A>T GRCh38
NC_000004.11:g.55991492A>T , CM000666.1:g.55991492A>T GRCh37
NC_000004.10:g.55686249A>T NCBI36
NG_012004.1:g.5271T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.-32T>A MANE Select ENSP00000263923.4:n.-32T>A
ENST00000263923.4:c.-32T>A ENSP00000263923.4:n.-32T>A
NM_002253.2:c.-32T>A NP_002244.1:n.-32T>A
NM_002253.3:c.-32T>A NP_002244.1:n.-32T>A
NM_002253.4:c.-32T>A MANE Select NP_002244.1:n.-32T>A
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