Canonical Allele Identifier: CA336132727

Gene: F9

Linked Data

• dbSNP Id: rs1032331792
• gnomAD v2: X-138623212-C-G
• gnomAD v3: X-139541053-C-G
• gnomAD v4: X-139541053-C-G
• MyVariant Identifiers: chrX:g.138623212C>G (hg19) ; chrX:g.139541053C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.139541053C>G , CM000685.2:g.139541053C>G	GRCh38
NC_000023.10:g.138623212C>G , CM000685.1:g.138623212C>G	GRCh37
NC_000023.9:g.138450878C>G	NCBI36
NG_007994.1:g.15318C>G , LRG_556:g.15318C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000218099.7:c.278-23C>G MANE Select	ENSP00000218099.2:n.278-23C>G
ENST00000218099.6:c.278-23C>G	ENSP00000218099.2:n.278-23C>G
ENST00000394090.2:c.277+3667C>G	ENSP00000377650.2:n.277+3667C>G
ENST00000479617.2:n.242-34C>G
NM_000133.3:c.278-23C>G , LRG_556t1:c.278-23C>G	NP_000124.1:n.278-23C>G
NM_001313913.1:c.277+3667C>G	NP_001300842.1:n.277+3667C>G
XM_005262397.3:c.278-23C>G	XP_005262454.1:n.278-23C>G
XM_005262397.4:c.278-23C>G	XP_005262454.1:n.278-23C>G
NM_000133.4:c.278-23C>G MANE Select	NP_000124.1:n.278-23C>G
NM_001313913.2:c.277+3667C>G	NP_001300842.1:n.277+3667C>G