Canonical Allele Identifier: CA439489614
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1490446016
gnomAD v2: 4-55991434-G-A
gnomAD v3: 4-55125267-G-A
gnomAD v4: 4-55125267-G-A
MyVariant Identifiers: chr4:g.55991434G>A (hg19) chr4:g.55125267G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125267G>A , CM000666.2:g.55125267G>A GRCh38
NC_000004.11:g.55991434G>A , CM000666.1:g.55991434G>A GRCh37
NC_000004.10:g.55686191G>A NCBI36
NG_012004.1:g.5329C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.27C>T MANE Select ENSP00000263923.4:p.Val9=
ENST00000263923.4:c.27C>T ENSP00000263923.4:p.Val9=
ENST00000512566.1:n.27C>T
NM_002253.2:c.27C>T NP_002244.1:p.Val9=
NM_002253.3:c.27C>T NP_002244.1:p.Val9=
NM_002253.4:c.27C>T MANE Select NP_002244.1:p.Val9=
Search 100 bp 5'
Search 100 bp 3'