Canonical Allele Identifier: CA2727473948
Gene: FLT1 HGNC NCBI

Linked Data

dbSNP Id: rs1448481489

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355529T>G , CM000675.2:g.28355529T>G GRCh38
NC_000013.10:g.28929666T>G , CM000675.1:g.28929666T>G GRCh37
NC_000013.9:g.27827666T>G NCBI36
NG_012003.1:g.144600A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282397.9:c.2248+2025A>C MANE Select ENSP00000282397.4:n.2248+2025A>C
ENST00000282397.8:c.2248+2025A>C ENSP00000282397.4:n.2248+2025A>C
NM_002019.4:c.2248+2025A>C MANE Select NP_002010.2:n.2248+2025A>C
XM_017020485.1:c.2248+2025A>C XP_016875974.1:n.2248+2025A>C