Canonical Allele Identifier: CA96921920
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs567997361
gnomAD v3: 4-55125414-A-C
gnomAD v4: 4-55125414-A-C
MyVariant Identifiers: chr4:g.55991581A>C (hg19) chr4:g.55125414A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125414A>C , CM000666.2:g.55125414A>C GRCh38
NC_000004.11:g.55991581A>C , CM000666.1:g.55991581A>C GRCh37
NC_000004.10:g.55686338A>C NCBI36
NG_012004.1:g.5182T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.-121T>G MANE Select ENSP00000263923.4:n.-121T>G
ENST00000263923.4:c.-121T>G ENSP00000263923.4:n.-121T>G
NM_002253.2:c.-121T>G NP_002244.1:n.-121T>G
NM_002253.3:c.-121T>G NP_002244.1:n.-121T>G
NM_002253.4:c.-121T>G MANE Select NP_002244.1:n.-121T>G
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