Canonical Allele Identifier: CA697059645
Gene: FLT1 HGNC NCBI

Linked Data

dbSNP Id: rs1439163046
MyVariant Identifiers: chr13:g.28929645T>A (hg19) chr13:g.28355508T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355508T>A , CM000675.2:g.28355508T>A GRCh38
NC_000013.10:g.28929645T>A , CM000675.1:g.28929645T>A GRCh37
NC_000013.9:g.27827645T>A NCBI36
NG_012003.1:g.144621A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000282397.9:c.2248+2046A>T MANE Select ENSP00000282397.4:n.2248+2046A>T
ENST00000282397.8:c.2248+2046A>T ENSP00000282397.4:n.2248+2046A>T
NM_002019.4:c.2248+2046A>T MANE Select NP_002010.2:n.2248+2046A>T
XM_017020485.1:c.2248+2046A>T XP_016875974.1:n.2248+2046A>T
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