Canonical Allele Identifier: CA2080959278
Gene: FLT1 HGNC NCBI

Linked Data

dbSNP Id: rs1872361741
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.28342165G>A , CM000675.2:g.28342165G>A GRCh38
NC_000013.10:g.28916302G>A , CM000675.1:g.28916302G>A GRCh37
NC_000013.9:g.27814302G>A NCBI36
NG_012003.1:g.157964C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000706527.1:n.181-2865C>T
ENST00000282397.9:c.2356-2865C>T MANE Select ENSP00000282397.4:n.2356-2865C>T
ENST00000282397.8:c.2356-2865C>T ENSP00000282397.4:n.2356-2865C>T
ENST00000540678.2:c.-1404-2865C>T ENSP00000443311.2:n.-1404-2865C>T
NM_002019.4:c.2356-2865C>T MANE Select NP_002010.2:n.2356-2865C>T
XM_017020485.1:c.2356-2865C>T XP_016875974.1:n.2356-2865C>T
Search 100 bp 5'
Search 100 bp 3'