Canonical Allele Identifier: CA343142083

Gene: F5

Linked Data

• gnomAD v4: 1-169572287-T-C
• MyVariant Identifiers: chr1:g.169541525T>C (hg19) ; chr1:g.169572287T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.169572287T>C , CM000663.2:g.169572287T>C	GRCh38
NC_000001.10:g.169541525T>C , CM000663.1:g.169541525T>C	GRCh37
NC_000001.9:g.167808149T>C	NCBI36
NG_011806.1:g.19245A>G , LRG_553:g.19245A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367797.9:c.307A>G MANE Select	ENSP00000356771.3:p.Lys103Glu
ENST00000367796.3:c.307A>G	ENSP00000356770.3:p.Lys103Glu
ENST00000367797.7:c.307A>G	ENSP00000356771.3:p.Lys103Glu
NM_000130.4:c.307A>G , LRG_553t1:c.307A>G	NP_000121.2:p.Lys103Glu
XM_017000660.2:c.-105A>G	XP_016856149.1:n.-105A>G
NM_000130.5:c.307A>G MANE Select	NP_000121.2:p.Lys103Glu