Canonical Allele Identifier: CA421930708

Gene: F5

Linked Data

• MyVariant Identifiers: chr1:g.169511072A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169541834A>G , CM000663.2:g.169541834A>G	GRCh38
NC_000001.10:g.169511072A>G , CM000663.1:g.169511072A>G	GRCh37
NC_000001.9:g.167777696A>G	NCBI36
NG_011806.1:g.49698T>C , LRG_553:g.49698T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.3256T>C MANE Select	ENSP00000356771.3:p.Leu1086=
ENST00000367796.3:c.3271T>C	ENSP00000356770.3:p.Leu1091=
ENST00000367797.7:c.3256T>C	ENSP00000356771.3:p.Leu1086=
NM_000130.4:c.3256T>C , LRG_553t1:c.3256T>C	NP_000121.2:p.Leu1086=
XM_017000660.2:c.2845T>C	XP_016856149.1:p.Leu949=
NM_000130.5:c.3256T>C MANE Select	NP_000121.2:p.Leu1086=