Canonical Allele Identifier: CA2080976317
Gene: FLT1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355603C= , CM000675.2:g.28355603C= GRCh38
NC_000013.10:g.28929740C= , CM000675.1:g.28929740C= GRCh37
NC_000013.9:g.27827740C= NCBI36
NG_012003.1:g.144526G=

Transcript Alleles

HGVS Amino-acid change
ENST00000282397.9:c.2248+1951G= MANE Select ENSP00000282397.4:n.2248+1951G=
ENST00000282397.8:c.2248+1951G= ENSP00000282397.4:n.2248+1951G=
NM_002019.4:c.2248+1951G= MANE Select NP_002010.2:n.2248+1951G=
XM_017020485.1:c.2248+1951G= XP_016875974.1:n.2248+1951G=
Search 100 bp 5'
Search 100 bp 3'