Canonical Allele Identifier: CA2080959379
Gene: FLT1 HGNC NCBI

Linked Data

dbSNP Id: rs1872366215
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28342230A>G , CM000675.2:g.28342230A>G GRCh38
NC_000013.10:g.28916367A>G , CM000675.1:g.28916367A>G GRCh37
NC_000013.9:g.27814367A>G NCBI36
NG_012003.1:g.157899T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706527.1:n.181-2930T>C
ENST00000282397.9:c.2356-2930T>C MANE Select ENSP00000282397.4:n.2356-2930T>C
ENST00000282397.8:c.2356-2930T>C ENSP00000282397.4:n.2356-2930T>C
ENST00000540678.2:c.-1404-2930T>C ENSP00000443311.2:n.-1404-2930T>C
NM_002019.4:c.2356-2930T>C MANE Select NP_002010.2:n.2356-2930T>C
XM_017020485.1:c.2356-2930T>C XP_016875974.1:n.2356-2930T>C
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