Canonical Allele Identifier: CA2925157
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs756900989
gnomAD v2: 4-55991376-C-T
gnomAD v3: 4-55125209-C-T
gnomAD v4: 4-55125209-C-T

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125209C>T , CM000666.2:g.55125209C>T GRCh38
NC_000004.11:g.55991376C>T , CM000666.1:g.55991376C>T GRCh37
NC_000004.10:g.55686133C>T NCBI36
NG_012004.1:g.5387G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000263923.5:c.67+18G>A MANE Select ENSP00000263923.4:n.67+18G>A
ENST00000263923.4:c.67+18G>A ENSP00000263923.4:n.67+18G>A
ENST00000512566.1:n.67+18G>A
NM_002253.2:c.67+18G>A NP_002244.1:n.67+18G>A
NM_002253.3:c.67+18G>A NP_002244.1:n.67+18G>A
NM_002253.4:c.67+18G>A MANE Select NP_002244.1:n.67+18G>A