Canonical Allele Identifier: CA2694839662

Gene: F9

Linked Data

• gnomAD v4: X-139551029-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139551029A>G , CM000685.2:g.139551029A>G	GRCh38
NC_000023.10:g.138633188A>G , CM000685.1:g.138633188A>G	GRCh37
NC_000023.9:g.138460854A>G	NCBI36
NG_007994.1:g.25294A>G , LRG_556:g.25294A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.521-33A>G MANE Select	ENSP00000218099.2:n.521-33A>G
ENST00000643157.1:n.1188-33A>G
ENST00000218099.6:c.521-33A>G	ENSP00000218099.2:n.521-33A>G
ENST00000394090.2:c.407-33A>G	ENSP00000377650.2:n.407-33A>G
NM_000133.3:c.521-33A>G , LRG_556t1:c.521-33A>G	NP_000124.1:n.521-33A>G
NM_001313913.1:c.407-33A>G	NP_001300842.1:n.407-33A>G
XM_005262397.3:c.392-33A>G	XP_005262454.1:n.392-33A>G
XM_005262397.4:c.392-33A>G	XP_005262454.1:n.392-33A>G
NM_000133.4:c.521-33A>G MANE Select	NP_000124.1:n.521-33A>G
NM_001313913.2:c.407-33A>G	NP_001300842.1:n.407-33A>G