Canonical Allele Identifier: CA697059649
Gene: FLT1 HGNC NCBI

Linked Data

dbSNP Id: rs1448481489
MyVariant Identifiers: chr13:g.28929666T>C (hg19) chr13:g.28355529T>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355529T>C , CM000675.2:g.28355529T>C GRCh38
NC_000013.10:g.28929666T>C , CM000675.1:g.28929666T>C GRCh37
NC_000013.9:g.27827666T>C NCBI36
NG_012003.1:g.144600A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000282397.9:c.2248+2025A>G MANE Select ENSP00000282397.4:n.2248+2025A>G
ENST00000282397.8:c.2248+2025A>G ENSP00000282397.4:n.2248+2025A>G
NM_002019.4:c.2248+2025A>G MANE Select NP_002010.2:n.2248+2025A>G
XM_017020485.1:c.2248+2025A>G XP_016875974.1:n.2248+2025A>G
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