Canonical Allele Identifier: CA96884134
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs758802040
gnomAD v2: 4-55957649-G-A
gnomAD v3: 4-55091482-G-A
gnomAD v4: 4-55091482-G-A

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55091482G>A , CM000666.2:g.55091482G>A GRCh38
NC_000004.11:g.55957649G>A , CM000666.1:g.55957649G>A GRCh37
NC_000004.10:g.55652406G>A NCBI36
NG_012004.1:g.39114C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000263923.5:c.3069+1135C>T MANE Select ENSP00000263923.4:n.3069+1135C>T
ENST00000647068.1:n.3082+1135C>T
ENST00000263923.4:c.3069+1135C>T ENSP00000263923.4:n.3069+1135C>T
NM_002253.2:c.3069+1135C>T NP_002244.1:n.3069+1135C>T
NM_002253.3:c.3069+1135C>T NP_002244.1:n.3069+1135C>T
NM_002253.4:c.3069+1135C>T MANE Select NP_002244.1:n.3069+1135C>T