Canonical Allele Identifier: CA2694839887

Gene: F9

Linked Data

• gnomAD v4: X-139561490-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139561490G>C , CM000685.2:g.139561490G>C	GRCh38
NC_000023.10:g.138643649G>C , CM000685.1:g.138643649G>C	GRCh37
NC_000023.9:g.138471315G>C	NCBI36
NG_007994.1:g.35755G>C , LRG_556:g.35755G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.839-34G>C MANE Select	ENSP00000218099.2:n.839-34G>C
ENST00000643157.1:n.1506-34G>C
ENST00000218099.6:c.839-34G>C	ENSP00000218099.2:n.839-34G>C
ENST00000394090.2:c.725-34G>C	ENSP00000377650.2:n.725-34G>C
NM_000133.3:c.839-34G>C , LRG_556t1:c.839-34G>C	NP_000124.1:n.839-34G>C
NM_001313913.1:c.725-34G>C	NP_001300842.1:n.725-34G>C
XM_005262397.3:c.710-34G>C	XP_005262454.1:n.710-34G>C
XM_005262397.4:c.710-34G>C	XP_005262454.1:n.710-34G>C
NM_000133.4:c.839-34G>C MANE Select	NP_000124.1:n.839-34G>C
NM_001313913.2:c.725-34G>C	NP_001300842.1:n.725-34G>C