Canonical Allele Identifier: CA695267744

Gene: F7

Linked Data

• dbSNP Id: rs1434181649
• gnomAD v4: 13-113118284-C-T
• MyVariant Identifiers: chr13:g.113772598C>T (hg19) ; chr13:g.113118284C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118284C>T , CM000675.2:g.113118284C>T	GRCh38
NC_000013.10:g.113772598C>T , CM000675.1:g.113772598C>T	GRCh37
NC_000013.9:g.112820599C>T	NCBI36
NG_009258.1:g.486C>T , LRG_548:g.486C>T
NG_009262.1:g.17494C>T , LRG_554:g.17494C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.740-129C>T MANE Select	ENSP00000329546.4:n.740-129C>T
ENST00000346342.7:c.740-129C>T	ENSP00000329546.3:n.740-129C>T
ENST00000375581.3:c.806-129C>T	ENSP00000364731.3:n.806-129C>T
ENST00000541084.5:c.554-129C>T	ENSP00000442051.2:n.554-129C>T
NM_000131.4:c.806-129C>T , LRG_554t1:c.806-129C>T	NP_000122.1:n.806-129C>T
NM_001267554.1:c.554-129C>T	NP_001254483.1:n.554-129C>T
NM_019616.3:c.740-129C>T , LRG_554t2:c.740-129C>T	NP_062562.1:n.740-129C>T
NR_051961.1:n.827-129C>T
XM_006719963.2:c.599-129C>T	XP_006720026.1:n.599-129C>T
XM_011537474.1:c.848-129C>T	XP_011535776.1:n.848-129C>T
XM_011537475.1:c.662-129C>T	XP_011535777.1:n.662-129C>T
XM_011537476.1:c.500-129C>T	XP_011535778.1:n.500-129C>T
XM_011537477.1:c.809-129C>T	XP_011535779.1:n.809-129C>T
XM_006719963.3:c.644-129C>T	XP_006720026.2:n.644-129C>T
XM_011537474.2:c.893-129C>T	XP_011535776.2:n.893-129C>T
XM_011537475.2:c.707-129C>T	XP_011535777.2:n.707-129C>T
XM_011537476.2:c.500-129C>T	XP_011535778.1:n.500-129C>T
NM_019616.4:c.740-129C>T MANE Select	NP_062562.1:n.740-129C>T
NR_051961.2:n.824-129C>T
NM_001267554.2:c.554-129C>T	NP_001254483.1:n.554-129C>T