Canonical Allele Identifier: CA388786193

Gene: F7

Linked Data

• dbSNP Id: rs2142233313
• MyVariant Identifiers: chr13:g.113772946G>A (hg19) ; chr13:g.113118632G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118632G>A , CM000675.2:g.113118632G>A	GRCh38
NC_000013.10:g.113772946G>A , CM000675.1:g.113772946G>A	GRCh37
NC_000013.9:g.112820947G>A	NCBI36
NG_009258.1:g.834G>A , LRG_548:g.834G>A
NG_009262.1:g.17842G>A , LRG_554:g.17842G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.959G>A MANE Select	ENSP00000329546.4:p.Ser320Asn
ENST00000346342.7:c.959G>A	ENSP00000329546.3:p.Ser320Asn
ENST00000375581.3:c.1025G>A	ENSP00000364731.3:p.Ser342Asn
ENST00000541084.5:c.773G>A	ENSP00000442051.2:p.Ser258Asn
NM_000131.4:c.1025G>A , LRG_554t1:c.1025G>A	NP_000122.1:p.Ser342Asn
NM_001267554.1:c.773G>A	NP_001254483.1:p.Ser258Asn
NM_019616.3:c.959G>A , LRG_554t2:c.959G>A	NP_062562.1:p.Ser320Asn
NR_051961.1:n.1046G>A
XM_006719963.2:c.818G>A	XP_006720026.1:p.Ser273Asn
XM_011537474.1:c.1067G>A	XP_011535776.1:p.Ser356Asn
XM_011537475.1:c.881G>A	XP_011535777.1:p.Ser294Asn
XM_011537476.1:c.719G>A	XP_011535778.1:p.Ser240Asn
XM_011537477.1:c.1028G>A	XP_011535779.1:p.Ser343Asn
XM_006719963.3:c.863G>A	XP_006720026.2:p.Ser288Asn
XM_011537474.2:c.1112G>A	XP_011535776.2:p.Ser371Asn
XM_011537475.2:c.926G>A	XP_011535777.2:p.Ser309Asn
XM_011537476.2:c.719G>A	XP_011535778.1:p.Ser240Asn
NM_019616.4:c.959G>A MANE Select	NP_062562.1:p.Ser320Asn
NR_051961.2:n.1043G>A
NM_001267554.2:c.773G>A	NP_001254483.1:p.Ser258Asn