Canonical Allele Identifier: CA2694839896

Gene: F9

Linked Data

• gnomAD v4: X-139562080-G-A

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562080G>A , CM000685.2:g.139562080G>A	GRCh38
NC_000023.10:g.138644239G>A , CM000685.1:g.138644239G>A	GRCh37
NC_000023.9:g.138471905G>A	NCBI36
NG_007994.1:g.36345G>A , LRG_556:g.36345G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.*9G>A MANE Select	ENSP00000218099.2:n.*9G>A
ENST00000643157.1:n.1723+339G>A
ENST00000218099.6:c.*9G>A	ENSP00000218099.2:n.*9G>A
NM_000133.3:c.*9G>A , LRG_556t1:c.*9G>A	NP_000124.1:n.*9G>A
NM_001313913.1:c.*9G>A	NP_001300842.1:n.*9G>A
XM_005262397.3:c.*9G>A	XP_005262454.1:n.*9G>A
XM_005262397.4:c.*9G>A	XP_005262454.1:n.*9G>A
NM_000133.4:c.*9G>A MANE Select	NP_000124.1:n.*9G>A
NM_001313913.2:c.*9G>A	NP_001300842.1:n.*9G>A