Canonical Allele Identifier: CA96922069

Gene: KDR

Linked Data

• dbSNP Id: rs572765398
• gnomAD v2: 4-55991658-A-C
• gnomAD v3: 4-55125491-A-C
• gnomAD v4: 4-55125491-A-C
• MyVariant Identifiers: chr4:g.55991658A>C (hg19) ; chr4:g.55125491A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.55125491A>C , CM000666.2:g.55125491A>C	GRCh38
NC_000004.11:g.55991658A>C , CM000666.1:g.55991658A>C	GRCh37
NC_000004.10:g.55686415A>C	NCBI36
NG_012004.1:g.5105T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000263923.5:c.-198T>G MANE Select	ENSP00000263923.4:n.-198T>G
ENST00000263923.4:c.-198T>G	ENSP00000263923.4:n.-198T>G
NM_002253.2:c.-198T>G	NP_002244.1:n.-198T>G
NM_002253.3:c.-198T>G	NP_002244.1:n.-198T>G
NM_002253.4:c.-198T>G MANE Select	NP_002244.1:n.-198T>G