Canonical Allele Identifier: CA5967121
Gene: F2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.46726627_46726710del , CM000673.2:g.46726627_46726710del GRCh38
NC_000011.9:g.46748177_46748260del , CM000673.1:g.46748177_46748260del GRCh37
NC_000011.8:g.46704753_46704836del NCBI36
NG_008953.1:g.12435_12518del , LRG_551:g.12435_12518del

Transcript Alleles

HGVS Amino-acid Change
ENST00000311907.10:c.1003+1_1004-1del
ENST00000311907.9:c.1003+1_1004-1del
ENST00000530231.5:c.1003+1_1004-1del
NM_000506.3:c.1003+1_1004-1del
NM_000506.4:c.1003+1_1004-1del , LRG_551t1:c.1003+1_1004-1del
NM_001311257.1:c.955+1_956-1del
XR_428840.2:n.1047+1_1048-1del
XR_428840.4:n.1038+1_1039-1del
NM_000506.5:c.1003+1_1004-1del
NM_001311257.2:c.955+1_956-1del