Canonical Allele Identifier: CA2080959271
Gene: FLT1 HGNC NCBI

Linked Data

dbSNP Id: rs1872361483
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28342160G>A , CM000675.2:g.28342160G>A GRCh38
NC_000013.10:g.28916297G>A , CM000675.1:g.28916297G>A GRCh37
NC_000013.9:g.27814297G>A NCBI36
NG_012003.1:g.157969C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000706527.1:n.181-2860C>T
ENST00000282397.9:c.2356-2860C>T MANE Select ENSP00000282397.4:n.2356-2860C>T
ENST00000282397.8:c.2356-2860C>T ENSP00000282397.4:n.2356-2860C>T
ENST00000540678.2:c.-1404-2860C>T ENSP00000443311.2:n.-1404-2860C>T
NM_002019.4:c.2356-2860C>T MANE Select NP_002010.2:n.2356-2860C>T
XM_017020485.1:c.2356-2860C>T XP_016875974.1:n.2356-2860C>T
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