Canonical Allele Identifier: CA1137751118

Gene: F9

Linked Data

• dbSNP Id: rs1928099160
• gnomAD v3: X-139561433-C-T
• gnomAD v4: X-139561433-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561433C>T , CM000685.2:g.139561433C>T	GRCh38
NC_000023.10:g.138643592C>T , CM000685.1:g.138643592C>T	GRCh37
NC_000023.9:g.138471258C>T	NCBI36
NG_007994.1:g.35698C>T , LRG_556:g.35698C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.839-91C>T MANE Select	ENSP00000218099.2:n.839-91C>T
ENST00000643157.1:n.1506-91C>T
ENST00000218099.6:c.839-91C>T	ENSP00000218099.2:n.839-91C>T
ENST00000394090.2:c.725-91C>T	ENSP00000377650.2:n.725-91C>T
NM_000133.3:c.839-91C>T , LRG_556t1:c.839-91C>T	NP_000124.1:n.839-91C>T
NM_001313913.1:c.725-91C>T	NP_001300842.1:n.725-91C>T
XM_005262397.3:c.710-91C>T	XP_005262454.1:n.710-91C>T
XM_005262397.4:c.710-91C>T	XP_005262454.1:n.710-91C>T
NM_000133.4:c.839-91C>T MANE Select	NP_000124.1:n.839-91C>T
NM_001313913.2:c.725-91C>T	NP_001300842.1:n.725-91C>T