Canonical Allele Identifier: CA2694839527

Gene: F9

Linked Data

• gnomAD v4: X-139548242-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139548242T>C , CM000685.2:g.139548242T>C	GRCh38
NC_000023.10:g.138630401T>C , CM000685.1:g.138630401T>C	GRCh37
NC_000023.9:g.138458067T>C	NCBI36
NG_007994.1:g.22507T>C , LRG_556:g.22507T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.392-121T>C MANE Select	ENSP00000218099.2:n.392-121T>C
ENST00000643157.1:n.1059-121T>C
ENST00000218099.6:c.392-121T>C	ENSP00000218099.2:n.392-121T>C
ENST00000394090.2:c.278-121T>C	ENSP00000377650.2:n.278-121T>C
ENST00000479617.2:n.345-121T>C
NM_000133.3:c.392-121T>C , LRG_556t1:c.392-121T>C	NP_000124.1:n.392-121T>C
NM_001313913.1:c.278-121T>C	NP_001300842.1:n.278-121T>C
XM_005262397.3:c.392-2820T>C	XP_005262454.1:n.392-2820T>C
XM_005262397.4:c.392-2820T>C	XP_005262454.1:n.392-2820T>C
NM_000133.4:c.392-121T>C MANE Select	NP_000124.1:n.392-121T>C
NM_001313913.2:c.278-121T>C	NP_001300842.1:n.278-121T>C