Canonical Allele Identifier: CA796416979
Gene: KDR HGNC NCBI

Linked Data

dbSNP Id: rs1406667358
MyVariant Identifiers: chr4:g.55953468G>A (hg19) chr4:g.55087301G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.55087301G>A , CM000666.2:g.55087301G>A GRCh38
NC_000004.11:g.55953468G>A , CM000666.1:g.55953468G>A GRCh37
NC_000004.10:g.55648225G>A NCBI36
NG_012004.1:g.43295C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000263923.5:c.3662+306C>T MANE Select ENSP00000263923.4:n.3662+306C>T
ENST00000647068.1:n.3675+306C>T
ENST00000263923.4:c.3662+306C>T ENSP00000263923.4:n.3662+306C>T
NM_002253.2:c.3662+306C>T NP_002244.1:n.3662+306C>T
NM_002253.3:c.3662+306C>T NP_002244.1:n.3662+306C>T
NM_002253.4:c.3662+306C>T MANE Select NP_002244.1:n.3662+306C>T
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