Canonical Allele Identifier: CA247328734
Gene: FLT1 HGNC NCBI

Linked Data

dbSNP Id: rs907296017
MyVariant Identifiers: chr13:g.28916327A>G (hg19) chr13:g.28342190A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28342190A>G , CM000675.2:g.28342190A>G GRCh38
NC_000013.10:g.28916327A>G , CM000675.1:g.28916327A>G GRCh37
NC_000013.9:g.27814327A>G NCBI36
NG_012003.1:g.157939T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000706527.1:n.181-2890T>C
ENST00000282397.9:c.2356-2890T>C MANE Select ENSP00000282397.4:n.2356-2890T>C
ENST00000282397.8:c.2356-2890T>C ENSP00000282397.4:n.2356-2890T>C
ENST00000540678.2:c.-1404-2890T>C ENSP00000443311.2:n.-1404-2890T>C
NM_002019.4:c.2356-2890T>C MANE Select NP_002010.2:n.2356-2890T>C
XM_017020485.1:c.2356-2890T>C XP_016875974.1:n.2356-2890T>C
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