Canonical Allele Identifier: CA96921879
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs919430835
gnomAD v4: 4-55125402-G-A
MyVariant Identifiers: chr4:g.55125402G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125402G>A , CM000666.2:g.55125402G>A GRCh38
NC_000004.11:g.55991569G>A , CM000666.1:g.55991569G>A GRCh37
NC_000004.10:g.55686326G>A NCBI36
NG_012004.1:g.5194C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.-109C>T MANE Select ENSP00000263923.4:n.-109C>T
ENST00000263923.4:c.-109C>T ENSP00000263923.4:n.-109C>T
NM_002253.2:c.-109C>T NP_002244.1:n.-109C>T
NM_002253.3:c.-109C>T NP_002244.1:n.-109C>T
NM_002253.4:c.-109C>T MANE Select NP_002244.1:n.-109C>T
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