Canonical Allele Identifier: CA1206146516
Gene: F5 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169552219T= , CM000663.2:g.169552219T= GRCh38
NC_000001.10:g.169521457T= , CM000663.1:g.169521457T= GRCh37
NC_000001.9:g.167788081T= NCBI36
NG_011806.1:g.39313A= , LRG_553:g.39313A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1296+338A= MANE Select ENSP00000356771.3:n.1296+338A=
ENST00000367796.3:c.1296+338A= ENSP00000356770.3:n.1296+338A=
ENST00000367797.7:c.1296+338A= ENSP00000356771.3:n.1296+338A=
NM_000130.4:c.1296+338A= , LRG_553t1:c.1296+338A= NP_000121.2:n.1296+338A=
XM_017000660.2:c.885+338A= XP_016856149.1:n.885+338A=
NM_000130.5:c.1296+338A= MANE Select NP_000121.2:n.1296+338A=
Search 100 bp 5'
Search 100 bp 3'