Canonical Allele Identifier: CA247338660
Gene: FLT1 HGNC NCBI

Linked Data

dbSNP Id: rs756245278
gnomAD v3: 13-28355527-G-A
gnomAD v4: 13-28355527-G-A
MyVariant Identifiers: chr13:g.28929664G>A (hg19) chr13:g.28355527G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355527G>A , CM000675.2:g.28355527G>A GRCh38
NC_000013.10:g.28929664G>A , CM000675.1:g.28929664G>A GRCh37
NC_000013.9:g.27827664G>A NCBI36
NG_012003.1:g.144602C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000282397.9:c.2248+2027C>T MANE Select ENSP00000282397.4:n.2248+2027C>T
ENST00000282397.8:c.2248+2027C>T ENSP00000282397.4:n.2248+2027C>T
NM_002019.4:c.2248+2027C>T MANE Select NP_002010.2:n.2248+2027C>T
XM_017020485.1:c.2248+2027C>T XP_016875974.1:n.2248+2027C>T
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