Canonical Allele Identifier: CA247338618
Gene: FLT1 HGNC NCBI

Linked Data

dbSNP Id: rs577210270

Genomic Alleles

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

Transcript Alleles

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