Canonical Allele Identifier: CA247338622
Gene: FLT1 HGNC NCBI

Linked Data

dbSNP Id: rs577210270

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355523C>T , CM000675.2:g.28355523C>T GRCh38
NC_000013.10:g.28929660C>T , CM000675.1:g.28929660C>T GRCh37
NC_000013.9:g.27827660C>T NCBI36
NG_012003.1:g.144606G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282397.9:c.2248+2031G>A MANE Select ENSP00000282397.4:n.2248+2031G>A
ENST00000282397.8:c.2248+2031G>A ENSP00000282397.4:n.2248+2031G>A
NM_002019.4:c.2248+2031G>A MANE Select NP_002010.2:n.2248+2031G>A
XM_017020485.1:c.2248+2031G>A XP_016875974.1:n.2248+2031G>A