Canonical Allele Identifier: CA1206136799
Gene: F5 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169532496G= , CM000663.2:g.169532496G= GRCh38
NC_000001.10:g.169501734G= , CM000663.1:g.169501734G= GRCh37
NC_000001.9:g.167768358G= NCBI36
NG_011806.1:g.59036C= , LRG_553:g.59036C=

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.4972-1474C= MANE Select ENSP00000356771.3:n.4972-1474C=
ENST00000367796.3:c.4987-1474C= ENSP00000356770.3:n.4987-1474C=
ENST00000367797.7:c.4972-1474C= ENSP00000356771.3:n.4972-1474C=
NM_000130.4:c.4972-1474C= , LRG_553t1:c.4972-1474C= NP_000121.2:n.4972-1474C=
XM_017000660.2:c.4561-1474C= XP_016856149.1:n.4561-1474C=
NM_000130.5:c.4972-1474C= MANE Select NP_000121.2:n.4972-1474C=
Search 100 bp 5'
Search 100 bp 3'