Canonical Allele Identifier: CA2694839928

Gene: F9

Linked Data

• gnomAD v4: X-139562180-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139562180G>T , CM000685.2:g.139562180G>T	GRCh38
NC_000023.10:g.138644339G>T , CM000685.1:g.138644339G>T	GRCh37
NC_000023.9:g.138472005G>T	NCBI36
NG_007994.1:g.36445G>T , LRG_556:g.36445G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.*109G>T MANE Select	ENSP00000218099.2:n.*109G>T
ENST00000643157.1:n.1723+439G>T
ENST00000218099.6:c.*109G>T	ENSP00000218099.2:n.*109G>T
NM_000133.3:c.*109G>T , LRG_556t1:c.*109G>T	NP_000124.1:n.*109G>T
NM_001313913.1:c.*109G>T	NP_001300842.1:n.*109G>T
XM_005262397.3:c.*109G>T	XP_005262454.1:n.*109G>T
XM_005262397.4:c.*109G>T	XP_005262454.1:n.*109G>T
NM_000133.4:c.*109G>T MANE Select	NP_000124.1:n.*109G>T
NM_001313913.2:c.*109G>T	NP_001300842.1:n.*109G>T