Canonical Allele Identifier: CA7059895

Gene: F7

Linked Data

• dbSNP Id: rs773173748
• ExAC: 13:113768049 C / T
• gnomAD v2: 13-113768049-C-T
• gnomAD v3: 13-113113735-C-T
• gnomAD v4: 13-113113735-C-T
• MyVariant Identifiers: chr13:g.113768049C>T (hg19) ; chr13:g.113113735C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113735C>T , CM000675.2:g.113113735C>T	GRCh38
NC_000013.10:g.113768049C>T , CM000675.1:g.113768049C>T	GRCh37
NC_000013.9:g.112816050C>T	NCBI36
NG_009262.1:g.12945C>T , LRG_554:g.12945C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.226-17C>T MANE Select	ENSP00000329546.4:n.226-17C>T
ENST00000346342.7:c.226-17C>T	ENSP00000329546.3:n.226-17C>T
ENST00000375581.3:c.292-17C>T	ENSP00000364731.3:n.292-17C>T
ENST00000444337.1:c.212-40C>T	ENSP00000387669.1:n.212-40C>T
ENST00000473085.1:n.173-17C>T
ENST00000479674.1:n.512-40C>T
ENST00000541084.5:c.65-112C>T	ENSP00000442051.2:n.65-112C>T
NM_000131.4:c.292-17C>T , LRG_554t1:c.292-17C>T	NP_000122.1:n.292-17C>T
NM_001267554.1:c.65-112C>T	NP_001254483.1:n.65-112C>T
NM_019616.3:c.226-17C>T , LRG_554t2:c.226-17C>T	NP_062562.1:n.226-17C>T
NR_051961.1:n.266-40C>T
XM_006719963.2:c.226-17C>T	XP_006720026.1:n.226-17C>T
XM_011537474.1:c.226-17C>T	XP_011535776.1:n.226-17C>T
XM_011537475.1:c.65-112C>T	XP_011535777.1:n.65-112C>T
XM_011537477.1:c.212-112C>T	XP_011535779.1:n.212-112C>T
XM_006719963.3:c.271-17C>T	XP_006720026.2:n.271-17C>T
XM_011537474.2:c.271-17C>T	XP_011535776.2:n.271-17C>T
XM_011537475.2:c.110-112C>T	XP_011535777.2:n.110-112C>T
NM_019616.4:c.226-17C>T MANE Select	NP_062562.1:n.226-17C>T
NR_051961.2:n.263-40C>T
NM_001267554.2:c.65-112C>T	NP_001254483.1:n.65-112C>T