Canonical Allele Identifier: CA954402950
Gene: FLT1 HGNC NCBI

Linked Data

dbSNP Id: rs1872870947
gnomAD v3: 13-28355603-C-T
gnomAD v4: 13-28355603-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355603C>T , CM000675.2:g.28355603C>T GRCh38
NC_000013.10:g.28929740C>T , CM000675.1:g.28929740C>T GRCh37
NC_000013.9:g.27827740C>T NCBI36
NG_012003.1:g.144526G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000282397.9:c.2248+1951G>A MANE Select ENSP00000282397.4:n.2248+1951G>A
ENST00000282397.8:c.2248+1951G>A ENSP00000282397.4:n.2248+1951G>A
NM_002019.4:c.2248+1951G>A MANE Select NP_002010.2:n.2248+1951G>A
XM_017020485.1:c.2248+1951G>A XP_016875974.1:n.2248+1951G>A
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