Canonical Allele Identifier: CA485423887

Gene: F7

Linked Data

• gnomAD v4: 13-113118534-C-T
• MyVariant Identifiers: chr13:g.113772848C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118534C>T , CM000675.2:g.113118534C>T	GRCh38
NC_000013.10:g.113772848C>T , CM000675.1:g.113772848C>T	GRCh37
NC_000013.9:g.112820849C>T	NCBI36
NG_009258.1:g.736C>T , LRG_548:g.736C>T
NG_009262.1:g.17744C>T , LRG_554:g.17744C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.861C>T MANE Select	ENSP00000329546.4:p.His287=
ENST00000346342.7:c.861C>T	ENSP00000329546.3:p.His287=
ENST00000375581.3:c.927C>T	ENSP00000364731.3:p.His309=
ENST00000541084.5:c.675C>T	ENSP00000442051.2:p.His225=
NM_000131.4:c.927C>T , LRG_554t1:c.927C>T	NP_000122.1:p.His309=
NM_001267554.1:c.675C>T	NP_001254483.1:p.His225=
NM_019616.3:c.861C>T , LRG_554t2:c.861C>T	NP_062562.1:p.His287=
NR_051961.1:n.948C>T
XM_006719963.2:c.720C>T	XP_006720026.1:p.His240=
XM_011537474.1:c.969C>T	XP_011535776.1:p.His323=
XM_011537475.1:c.783C>T	XP_011535777.1:p.His261=
XM_011537476.1:c.621C>T	XP_011535778.1:p.His207=
XM_011537477.1:c.930C>T	XP_011535779.1:p.His310=
XM_006719963.3:c.765C>T	XP_006720026.2:p.His255=
XM_011537474.2:c.1014C>T	XP_011535776.2:p.His338=
XM_011537475.2:c.828C>T	XP_011535777.2:p.His276=
XM_011537476.2:c.621C>T	XP_011535778.1:p.His207=
NM_019616.4:c.861C>T MANE Select	NP_062562.1:p.His287=
NR_051961.2:n.945C>T
NM_001267554.2:c.675C>T	NP_001254483.1:p.His225=