Canonical Allele Identifier: CA388785820

Gene: F7

Linked Data

• dbSNP Id: rs1163238422
• gnomAD v2: 13-113772754-G-A
• gnomAD v4: 13-113118440-G-A
• MyVariant Identifiers: chr13:g.113772754G>A (hg19) ; chr13:g.113118440G>A (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.767G>A MANE Select	ENSP00000329546.4:p.Gly256Glu
ENST00000346342.7:c.767G>A	ENSP00000329546.3:p.Gly256Glu
ENST00000375581.3:c.833G>A	ENSP00000364731.3:p.Gly278Glu
ENST00000541084.5:c.581G>A	ENSP00000442051.2:p.Gly194Glu
NM_000131.4:c.833G>A , LRG_554t1:c.833G>A	NP_000122.1:p.Gly278Glu
NM_001267554.1:c.581G>A	NP_001254483.1:p.Gly194Glu
NM_019616.3:c.767G>A , LRG_554t2:c.767G>A	NP_062562.1:p.Gly256Glu
NR_051961.1:n.854G>A
XM_006719963.2:c.626G>A	XP_006720026.1:p.Gly209Glu
XM_011537474.1:c.875G>A	XP_011535776.1:p.Gly292Glu
XM_011537475.1:c.689G>A	XP_011535777.1:p.Gly230Glu
XM_011537476.1:c.527G>A	XP_011535778.1:p.Gly176Glu
XM_011537477.1:c.836G>A	XP_011535779.1:p.Gly279Glu
XM_006719963.3:c.671G>A	XP_006720026.2:p.Gly224Glu
XM_011537474.2:c.920G>A	XP_011535776.2:p.Gly307Glu
XM_011537475.2:c.734G>A	XP_011535777.2:p.Gly245Glu
XM_011537476.2:c.527G>A	XP_011535778.1:p.Gly176Glu
NM_019616.4:c.767G>A MANE Select	NP_062562.1:p.Gly256Glu
NR_051961.2:n.851G>A
NM_001267554.2:c.581G>A	NP_001254483.1:p.Gly194Glu