Canonical Allele Identifier: CA551376990
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1414387516
gnomAD v2: 4-55953463-C-T
gnomAD v3: 4-55087296-C-T
gnomAD v4: 4-55087296-C-T
MyVariant Identifiers: chr4:g.55953463C>T (hg19) chr4:g.55087296C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55087296C>T , CM000666.2:g.55087296C>T GRCh38
NC_000004.11:g.55953463C>T , CM000666.1:g.55953463C>T GRCh37
NC_000004.10:g.55648220C>T NCBI36
NG_012004.1:g.43300G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3662+311G>A MANE Select ENSP00000263923.4:n.3662+311G>A
ENST00000647068.1:n.3675+311G>A
ENST00000263923.4:c.3662+311G>A ENSP00000263923.4:n.3662+311G>A
NM_002253.2:c.3662+311G>A NP_002244.1:n.3662+311G>A
NM_002253.3:c.3662+311G>A NP_002244.1:n.3662+311G>A
NM_002253.4:c.3662+311G>A MANE Select NP_002244.1:n.3662+311G>A
Search 100 bp 5'
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