Canonical Allele Identifier: CA388785822

Gene: F7

Linked Data

• gnomAD v4: 13-113118440-G-T
• MyVariant Identifiers: chr13:g.113772754G>T (hg19) ; chr13:g.113118440G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118440G>T , CM000675.2:g.113118440G>T	GRCh38
NC_000013.10:g.113772754G>T , CM000675.1:g.113772754G>T	GRCh37
NC_000013.9:g.112820755G>T	NCBI36
NG_009258.1:g.642G>T , LRG_548:g.642G>T
NG_009262.1:g.17650G>T , LRG_554:g.17650G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.767G>T MANE Select	ENSP00000329546.4:p.Gly256Val
ENST00000346342.7:c.767G>T	ENSP00000329546.3:p.Gly256Val
ENST00000375581.3:c.833G>T	ENSP00000364731.3:p.Gly278Val
ENST00000541084.5:c.581G>T	ENSP00000442051.2:p.Gly194Val
NM_000131.4:c.833G>T , LRG_554t1:c.833G>T	NP_000122.1:p.Gly278Val
NM_001267554.1:c.581G>T	NP_001254483.1:p.Gly194Val
NM_019616.3:c.767G>T , LRG_554t2:c.767G>T	NP_062562.1:p.Gly256Val
NR_051961.1:n.854G>T
XM_006719963.2:c.626G>T	XP_006720026.1:p.Gly209Val
XM_011537474.1:c.875G>T	XP_011535776.1:p.Gly292Val
XM_011537475.1:c.689G>T	XP_011535777.1:p.Gly230Val
XM_011537476.1:c.527G>T	XP_011535778.1:p.Gly176Val
XM_011537477.1:c.836G>T	XP_011535779.1:p.Gly279Val
XM_006719963.3:c.671G>T	XP_006720026.2:p.Gly224Val
XM_011537474.2:c.920G>T	XP_011535776.2:p.Gly307Val
XM_011537475.2:c.734G>T	XP_011535777.2:p.Gly245Val
XM_011537476.2:c.527G>T	XP_011535778.1:p.Gly176Val
NM_019616.4:c.767G>T MANE Select	NP_062562.1:p.Gly256Val
NR_051961.2:n.851G>T
NM_001267554.2:c.581G>T	NP_001254483.1:p.Gly194Val