Canonical Allele Identifier: CA2694839191

Gene: F9

Linked Data

• gnomAD v4: X-139541060-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541060T>C , CM000685.2:g.139541060T>C	GRCh38
NC_000023.10:g.138623219T>C , CM000685.1:g.138623219T>C	GRCh37
NC_000023.9:g.138450885T>C	NCBI36
NG_007994.1:g.15325T>C , LRG_556:g.15325T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000218099.7:c.278-16T>C MANE Select	ENSP00000218099.2:n.278-16T>C
ENST00000218099.6:c.278-16T>C	ENSP00000218099.2:n.278-16T>C
ENST00000394090.2:c.277+3674T>C	ENSP00000377650.2:n.277+3674T>C
ENST00000479617.2:n.242-27T>C
NM_000133.3:c.278-16T>C , LRG_556t1:c.278-16T>C	NP_000124.1:n.278-16T>C
NM_001313913.1:c.277+3674T>C	NP_001300842.1:n.277+3674T>C
XM_005262397.3:c.278-16T>C	XP_005262454.1:n.278-16T>C
XM_005262397.4:c.278-16T>C	XP_005262454.1:n.278-16T>C
NM_000133.4:c.278-16T>C MANE Select	NP_000124.1:n.278-16T>C
NM_001313913.2:c.277+3674T>C	NP_001300842.1:n.277+3674T>C