Canonical Allele Identifier: CA32390520
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs963239688

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169555109C>A , CM000663.2:g.169555109C>A GRCh38
NC_000001.10:g.169524347C>A , CM000663.1:g.169524347C>A GRCh37
NC_000001.9:g.167790971C>A NCBI36
NG_011806.1:g.36423G>T , LRG_553:g.36423G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1118+73G>T MANE Select ENSP00000356771.3:n.1118+73G>T
ENST00000367796.3:c.1118+73G>T ENSP00000356770.3:n.1118+73G>T
ENST00000367797.7:c.1118+73G>T ENSP00000356771.3:n.1118+73G>T
NM_000130.4:c.1118+73G>T , LRG_553t1:c.1118+73G>T NP_000121.2:n.1118+73G>T
XM_017000660.2:c.707+73G>T XP_016856149.1:n.707+73G>T
NM_000130.5:c.1118+73G>T MANE Select NP_000121.2:n.1118+73G>T