Canonical Allele Identifier: CA551381363
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1358953486
gnomAD v2: 4-55978999-T-C
gnomAD v3: 4-55112832-T-C
gnomAD v4: 4-55112832-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55112832T>C , CM000666.2:g.55112832T>C GRCh38
NC_000004.11:g.55978999T>C , CM000666.1:g.55978999T>C GRCh37
NC_000004.10:g.55673756T>C NCBI36
NG_012004.1:g.17764A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000263923.5:c.976+472A>G MANE Select ENSP00000263923.4:n.976+472A>G
ENST00000647068.1:n.989+472A>G
ENST00000263923.4:c.976+472A>G ENSP00000263923.4:n.976+472A>G
ENST00000512566.1:n.976+472A>G
NM_002253.2:c.976+472A>G NP_002244.1:n.976+472A>G
NM_002253.3:c.976+472A>G NP_002244.1:n.976+472A>G
NM_002253.4:c.976+472A>G MANE Select NP_002244.1:n.976+472A>G