Canonical Allele Identifier: CA697059639
Gene: FLT1 HGNC NCBI

Linked Data

dbSNP Id: rs1379273384
MyVariant Identifiers: chr13:g.28929628A>T (hg19) chr13:g.28355491A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28355491A>T , CM000675.2:g.28355491A>T GRCh38
NC_000013.10:g.28929628A>T , CM000675.1:g.28929628A>T GRCh37
NC_000013.9:g.27827628A>T NCBI36
NG_012003.1:g.144638T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000282397.9:c.2248+2063T>A MANE Select ENSP00000282397.4:n.2248+2063T>A
ENST00000282397.8:c.2248+2063T>A ENSP00000282397.4:n.2248+2063T>A
NM_002019.4:c.2248+2063T>A MANE Select NP_002010.2:n.2248+2063T>A
XM_017020485.1:c.2248+2063T>A XP_016875974.1:n.2248+2063T>A
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