Canonical Allele Identifier: CA485423825

Gene: F7

Linked Data

• dbSNP Id: rs1363918233
• gnomAD v2: 13-113772755-G-T
• gnomAD v4: 13-113118441-G-T
• MyVariant Identifiers: chr13:g.113772755G>T (hg19) ; chr13:g.113118441G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118441G>T , CM000675.2:g.113118441G>T	GRCh38
NC_000013.10:g.113772755G>T , CM000675.1:g.113772755G>T	GRCh37
NC_000013.9:g.112820756G>T	NCBI36
NG_009258.1:g.643G>T , LRG_548:g.643G>T
NG_009262.1:g.17651G>T , LRG_554:g.17651G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.768G>T MANE Select	ENSP00000329546.4:p.Gly256=
ENST00000346342.7:c.768G>T	ENSP00000329546.3:p.Gly256=
ENST00000375581.3:c.834G>T	ENSP00000364731.3:p.Gly278=
ENST00000541084.5:c.582G>T	ENSP00000442051.2:p.Gly194=
NM_000131.4:c.834G>T , LRG_554t1:c.834G>T	NP_000122.1:p.Gly278=
NM_001267554.1:c.582G>T	NP_001254483.1:p.Gly194=
NM_019616.3:c.768G>T , LRG_554t2:c.768G>T	NP_062562.1:p.Gly256=
NR_051961.1:n.855G>T
XM_006719963.2:c.627G>T	XP_006720026.1:p.Gly209=
XM_011537474.1:c.876G>T	XP_011535776.1:p.Gly292=
XM_011537475.1:c.690G>T	XP_011535777.1:p.Gly230=
XM_011537476.1:c.528G>T	XP_011535778.1:p.Gly176=
XM_011537477.1:c.837G>T	XP_011535779.1:p.Gly279=
XM_006719963.3:c.672G>T	XP_006720026.2:p.Gly224=
XM_011537474.2:c.921G>T	XP_011535776.2:p.Gly307=
XM_011537475.2:c.735G>T	XP_011535777.2:p.Gly245=
XM_011537476.2:c.528G>T	XP_011535778.1:p.Gly176=
NM_019616.4:c.768G>T MANE Select	NP_062562.1:p.Gly256=
NR_051961.2:n.852G>T
NM_001267554.2:c.582G>T	NP_001254483.1:p.Gly194=