Canonical Allele Identifier: CA2670674210
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1721007132
gnomAD v4: 4-55125397-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125397G>T , CM000666.2:g.55125397G>T GRCh38
NC_000004.11:g.55991564G>T , CM000666.1:g.55991564G>T GRCh37
NC_000004.10:g.55686321G>T NCBI36
NG_012004.1:g.5199C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.-104C>A MANE Select ENSP00000263923.4:n.-104C>A
ENST00000263923.4:c.-104C>A ENSP00000263923.4:n.-104C>A
NM_002253.2:c.-104C>A NP_002244.1:n.-104C>A
NM_002253.3:c.-104C>A NP_002244.1:n.-104C>A
NM_002253.4:c.-104C>A MANE Select NP_002244.1:n.-104C>A