Canonical Allele Identifier: CA421738213
Gene: F5 HGNC NCBI

Linked Data

MyVariant Identifiers: chr1:g.169541493A>G (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169572255A>G , CM000663.2:g.169572255A>G GRCh38
NC_000001.10:g.169541493A>G , CM000663.1:g.169541493A>G GRCh37
NC_000001.9:g.167808117A>G NCBI36
NG_011806.1:g.19277T>C , LRG_553:g.19277T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.339T>C MANE Select ENSP00000356771.3:p.His113=
ENST00000367796.3:c.339T>C ENSP00000356770.3:p.His113=
ENST00000367797.7:c.339T>C ENSP00000356771.3:p.His113=
NM_000130.4:c.339T>C , LRG_553t1:c.339T>C NP_000121.2:p.His113=
XM_017000660.2:c.-73T>C XP_016856149.1:n.-73T>C
NM_000130.5:c.339T>C MANE Select NP_000121.2:p.His113=