Canonical Allele Identifier: CA2727792275
Gene: FLT1 HGNC NCBI

Linked Data

dbSNP Id: rs2138870287

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355504T>G , CM000675.2:g.28355504T>G GRCh38
NC_000013.10:g.28929641T>G , CM000675.1:g.28929641T>G GRCh37
NC_000013.9:g.27827641T>G NCBI36
NG_012003.1:g.144625A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000282397.9:c.2248+2050A>C MANE Select ENSP00000282397.4:n.2248+2050A>C
ENST00000282397.8:c.2248+2050A>C ENSP00000282397.4:n.2248+2050A>C
NM_002019.4:c.2248+2050A>C MANE Select NP_002010.2:n.2248+2050A>C
XM_017020485.1:c.2248+2050A>C XP_016875974.1:n.2248+2050A>C