Canonical Allele Identifier: CA247318694
Gene: FLT1 HGNC NCBI

Linked Data

dbSNP Id: rs17619601
gnomAD v2: 13-28900510-C-T
gnomAD v3: 13-28326373-C-T
gnomAD v4: 13-28326373-C-T
MyVariant Identifiers: chr13:g.28900510C>T (hg19) chr13:g.28326373C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28326373C>T , CM000675.2:g.28326373C>T GRCh38
NC_000013.10:g.28900510C>T , CM000675.1:g.28900510C>T GRCh37
NC_000013.9:g.27798510C>T NCBI36
NG_012003.1:g.173756G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000706527.1:n.621+1089G>A
ENST00000282397.9:c.2796+1089G>A MANE Select ENSP00000282397.4:n.2796+1089G>A
ENST00000282397.8:c.2796+1089G>A ENSP00000282397.4:n.2796+1089G>A
ENST00000540678.2:c.-964+1089G>A ENSP00000443311.2:n.-964+1089G>A
ENST00000615611.4:c.81+1089G>A ENSP00000484385.1:n.81+1089G>A
NM_002019.4:c.2796+1089G>A MANE Select NP_002010.2:n.2796+1089G>A
XR_941798.1:n.918-2248C>T
XM_017020485.1:c.2682+1089G>A XP_016875974.1:n.2682+1089G>A
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