Canonical Allele Identifier: CA439632010
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs2110027570
MyVariant Identifiers: chr4:g.55976706G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55110539G>A , CM000666.2:g.55110539G>A GRCh38
NC_000004.11:g.55976706G>A , CM000666.1:g.55976706G>A GRCh37
NC_000004.10:g.55671463G>A NCBI36
NG_012004.1:g.20057C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.1119C>T MANE Select ENSP00000263923.4:p.Ser373=
ENST00000647068.1:n.1132C>T
ENST00000263923.4:c.1119C>T ENSP00000263923.4:p.Ser373=
ENST00000512566.1:n.1119C>T
NM_002253.2:c.1119C>T NP_002244.1:p.Ser373=
NM_002253.3:c.1119C>T NP_002244.1:p.Ser373=
NM_002253.4:c.1119C>T MANE Select NP_002244.1:p.Ser373=
Search 100 bp 5'
Search 100 bp 3'