Canonical Allele Identifier: CA914950163
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1560526747
gnomAD v2: 4-55991088-T-C
gnomAD v3: 4-55124921-T-C
gnomAD v4: 4-55124921-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55124921T>C , CM000666.2:g.55124921T>C GRCh38
NC_000004.11:g.55991088T>C , CM000666.1:g.55991088T>C GRCh37
NC_000004.10:g.55685845T>C NCBI36
NG_012004.1:g.5675A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.67+306A>G MANE Select ENSP00000263923.4:n.67+306A>G
ENST00000263923.4:c.67+306A>G ENSP00000263923.4:n.67+306A>G
ENST00000512566.1:n.67+306A>G
NM_002253.2:c.67+306A>G NP_002244.1:n.67+306A>G
NM_002253.3:c.67+306A>G NP_002244.1:n.67+306A>G
NM_002253.4:c.67+306A>G MANE Select NP_002244.1:n.67+306A>G