Canonical Allele Identifier: CA2694839782

Gene: F9

Linked Data

• gnomAD v4: X-139560877-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139560877T>C , CM000685.2:g.139560877T>C	GRCh38
NC_000023.10:g.138643036T>C , CM000685.1:g.138643036T>C	GRCh37
NC_000023.9:g.138470702T>C	NCBI36
NG_007994.1:g.35142T>C , LRG_556:g.35142T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.838+22T>C MANE Select	ENSP00000218099.2:n.838+22T>C
ENST00000643157.1:n.1505+22T>C
ENST00000218099.6:c.838+22T>C	ENSP00000218099.2:n.838+22T>C
ENST00000394090.2:c.724+22T>C	ENSP00000377650.2:n.724+22T>C
NM_000133.3:c.838+22T>C , LRG_556t1:c.838+22T>C	NP_000124.1:n.838+22T>C
NM_001313913.1:c.724+22T>C	NP_001300842.1:n.724+22T>C
XM_005262397.3:c.709+22T>C	XP_005262454.1:n.709+22T>C
XM_005262397.4:c.709+22T>C	XP_005262454.1:n.709+22T>C
NM_000133.4:c.838+22T>C MANE Select	NP_000124.1:n.838+22T>C
NM_001313913.2:c.724+22T>C	NP_001300842.1:n.724+22T>C