Canonical Allele Identifier: CA13873744
Gene: FLT1 HGNC NCBI

Linked Data

dbSNP Id: rs7324547
gnomAD v2: 13-28929607-A-G
gnomAD v3: 13-28355470-A-G
gnomAD v4: 13-28355470-A-G
MyVariant Identifiers: chr13:g.28929607A>G (hg19) chr13:g.28355470A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355470A>G , CM000675.2:g.28355470A>G GRCh38
NC_000013.10:g.28929607A>G , CM000675.1:g.28929607A>G GRCh37
NC_000013.9:g.27827607A>G NCBI36
NG_012003.1:g.144659T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000282397.9:c.2248+2084T>C MANE Select ENSP00000282397.4:n.2248+2084T>C
ENST00000282397.8:c.2248+2084T>C ENSP00000282397.4:n.2248+2084T>C
NM_002019.4:c.2248+2084T>C MANE Select NP_002010.2:n.2248+2084T>C
XM_017020485.1:c.2248+2084T>C XP_016875974.1:n.2248+2084T>C
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