Canonical Allele Identifier: CA796406997
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1164217818
gnomAD v3: 4-55124978-G-T
gnomAD v4: 4-55124978-G-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55124978G>T , CM000666.2:g.55124978G>T GRCh38
NC_000004.11:g.55991145G>T , CM000666.1:g.55991145G>T GRCh37
NC_000004.10:g.55685902G>T NCBI36
NG_012004.1:g.5618C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.67+249C>A MANE Select ENSP00000263923.4:n.67+249C>A
ENST00000263923.4:c.67+249C>A ENSP00000263923.4:n.67+249C>A
ENST00000512566.1:n.67+249C>A
NM_002253.2:c.67+249C>A NP_002244.1:n.67+249C>A
NM_002253.3:c.67+249C>A NP_002244.1:n.67+249C>A
NM_002253.4:c.67+249C>A MANE Select NP_002244.1:n.67+249C>A