Canonical Allele Identifier: CA96922185
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs986335112
gnomAD v4: 4-55125571-C-G

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55125571C>G , CM000666.2:g.55125571C>G GRCh38
NC_000004.11:g.55991738C>G , CM000666.1:g.55991738C>G GRCh37
NC_000004.10:g.55686495C>G NCBI36
NG_012004.1:g.5025G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.-278G>C MANE Select ENSP00000263923.4:n.-278G>C
ENST00000263923.4:c.-278G>C ENSP00000263923.4:n.-278G>C
NM_002253.2:c.-278G>C NP_002244.1:n.-278G>C
NM_002253.3:c.-278G>C NP_002244.1:n.-278G>C
NM_002253.4:c.-278G>C MANE Select NP_002244.1:n.-278G>C