Canonical Allele Identifier: CA2694839814

Gene: F9

Linked Data

• gnomAD v4: X-139560979-C-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560979C>A , CM000685.2:g.139560979C>A	GRCh38
NC_000023.10:g.138643138C>A , CM000685.1:g.138643138C>A	GRCh37
NC_000023.9:g.138470804C>A	NCBI36
NG_007994.1:g.35244C>A , LRG_556:g.35244C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.838+124C>A MANE Select	ENSP00000218099.2:n.838+124C>A
ENST00000643157.1:n.1505+124C>A
ENST00000218099.6:c.838+124C>A	ENSP00000218099.2:n.838+124C>A
ENST00000394090.2:c.724+124C>A	ENSP00000377650.2:n.724+124C>A
NM_000133.3:c.838+124C>A , LRG_556t1:c.838+124C>A	NP_000124.1:n.838+124C>A
NM_001313913.1:c.724+124C>A	NP_001300842.1:n.724+124C>A
XM_005262397.3:c.709+124C>A	XP_005262454.1:n.709+124C>A
XM_005262397.4:c.709+124C>A	XP_005262454.1:n.709+124C>A
NM_000133.4:c.838+124C>A MANE Select	NP_000124.1:n.838+124C>A
NM_001313913.2:c.724+124C>A	NP_001300842.1:n.724+124C>A