Canonical Allele Identifier: CA2727792275

Gene: FLT1

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