Canonical Allele Identifier: CA960396831

Gene: F7

Linked Data

• dbSNP Id: rs2036232522
• gnomAD v3: 13-113118340-A-G
• gnomAD v4: 13-113118340-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118340A>G , CM000675.2:g.113118340A>G	GRCh38
NC_000013.10:g.113772654A>G , CM000675.1:g.113772654A>G	GRCh37
NC_000013.9:g.112820655A>G	NCBI36
NG_009258.1:g.542A>G , LRG_548:g.542A>G
NG_009262.1:g.17550A>G , LRG_554:g.17550A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.740-73A>G MANE Select	ENSP00000329546.4:n.740-73A>G
ENST00000346342.7:c.740-73A>G	ENSP00000329546.3:n.740-73A>G
ENST00000375581.3:c.806-73A>G	ENSP00000364731.3:n.806-73A>G
ENST00000541084.5:c.554-73A>G	ENSP00000442051.2:n.554-73A>G
NM_000131.4:c.806-73A>G , LRG_554t1:c.806-73A>G	NP_000122.1:n.806-73A>G
NM_001267554.1:c.554-73A>G	NP_001254483.1:n.554-73A>G
NM_019616.3:c.740-73A>G , LRG_554t2:c.740-73A>G	NP_062562.1:n.740-73A>G
NR_051961.1:n.827-73A>G
XM_006719963.2:c.599-73A>G	XP_006720026.1:n.599-73A>G
XM_011537474.1:c.848-73A>G	XP_011535776.1:n.848-73A>G
XM_011537475.1:c.662-73A>G	XP_011535777.1:n.662-73A>G
XM_011537476.1:c.500-73A>G	XP_011535778.1:n.500-73A>G
XM_011537477.1:c.809-73A>G	XP_011535779.1:n.809-73A>G
XM_006719963.3:c.644-73A>G	XP_006720026.2:n.644-73A>G
XM_011537474.2:c.893-73A>G	XP_011535776.2:n.893-73A>G
XM_011537475.2:c.707-73A>G	XP_011535777.2:n.707-73A>G
XM_011537476.2:c.500-73A>G	XP_011535778.1:n.500-73A>G
NM_019616.4:c.740-73A>G MANE Select	NP_062562.1:n.740-73A>G
NR_051961.2:n.824-73A>G
NM_001267554.2:c.554-73A>G	NP_001254483.1:n.554-73A>G