Canonical Allele Identifier: CA697059648
Gene: FLT1 HGNC NCBI

Linked Data

dbSNP Id: rs756245278

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355527G>T , CM000675.2:g.28355527G>T GRCh38
NC_000013.10:g.28929664G>T , CM000675.1:g.28929664G>T GRCh37
NC_000013.9:g.27827664G>T NCBI36
NG_012003.1:g.144602C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000282397.9:c.2248+2027C>A MANE Select ENSP00000282397.4:n.2248+2027C>A
ENST00000282397.8:c.2248+2027C>A ENSP00000282397.4:n.2248+2027C>A
NM_002019.4:c.2248+2027C>A MANE Select NP_002010.2:n.2248+2027C>A
XM_017020485.1:c.2248+2027C>A XP_016875974.1:n.2248+2027C>A