Canonical Allele Identifier: CA356921334
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1170484244
gnomAD v2: 4-55991394-C-T
gnomAD v4: 4-55125227-C-T
MyVariant Identifiers: chr4:g.55991394C>T (hg19) chr4:g.55125227C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125227C>T , CM000666.2:g.55125227C>T GRCh38
NC_000004.11:g.55991394C>T , CM000666.1:g.55991394C>T GRCh37
NC_000004.10:g.55686151C>T NCBI36
NG_012004.1:g.5369G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.67G>A MANE Select ENSP00000263923.4:p.Gly23Ser
ENST00000263923.4:c.67G>A ENSP00000263923.4:p.Gly23Ser
ENST00000512566.1:n.67G>A
NM_002253.2:c.67G>A NP_002244.1:p.Gly23Ser
NM_002253.3:c.67G>A NP_002244.1:p.Gly23Ser
NM_002253.4:c.67G>A MANE Select NP_002244.1:p.Gly23Ser
Search 100 bp 5'
Search 100 bp 3'