Canonical Allele Identifier: CA96922184
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs943654217
gnomAD v2: 4-55991737-G-T
gnomAD v3: 4-55125570-G-T
gnomAD v4: 4-55125570-G-T
MyVariant Identifiers: chr4:g.55991737G>T (hg19) chr4:g.55125570G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125570G>T , CM000666.2:g.55125570G>T GRCh38
NC_000004.11:g.55991737G>T , CM000666.1:g.55991737G>T GRCh37
NC_000004.10:g.55686494G>T NCBI36
NG_012004.1:g.5026C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.-277C>A MANE Select ENSP00000263923.4:n.-277C>A
ENST00000263923.4:c.-277C>A ENSP00000263923.4:n.-277C>A
NM_002253.2:c.-277C>A NP_002244.1:n.-277C>A
NM_002253.3:c.-277C>A NP_002244.1:n.-277C>A
NM_002253.4:c.-277C>A MANE Select NP_002244.1:n.-277C>A
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