Canonical Allele Identifier: CA96887208
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs995918989
gnomAD v3: 4-55091841-G-A
gnomAD v4: 4-55091841-G-A
MyVariant Identifiers: chr4:g.55958008G>A (hg19) chr4:g.55091841G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091841G>A , CM000666.2:g.55091841G>A GRCh38
NC_000004.11:g.55958008G>A , CM000666.1:g.55958008G>A GRCh37
NC_000004.10:g.55652765G>A NCBI36
NG_012004.1:g.38755C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3069+776C>T MANE Select ENSP00000263923.4:n.3069+776C>T
ENST00000647068.1:n.3082+776C>T
ENST00000263923.4:c.3069+776C>T ENSP00000263923.4:n.3069+776C>T
NM_002253.2:c.3069+776C>T NP_002244.1:n.3069+776C>T
NM_002253.3:c.3069+776C>T NP_002244.1:n.3069+776C>T
NM_002253.4:c.3069+776C>T MANE Select NP_002244.1:n.3069+776C>T
Search 100 bp 5'
Search 100 bp 3'