Canonical Allele Identifier: CA7060136

Gene: F7

Linked Data

• dbSNP Id: rs779198014
• ExAC: 13:113772751 A / G
• gnomAD v2: 13-113772751-A-G
• gnomAD v3: 13-113118437-A-G
• gnomAD v4: 13-113118437-A-G
• MyVariant Identifiers: chr13:g.113772751A>G (hg19) ; chr13:g.113118437A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118437A>G , CM000675.2:g.113118437A>G	GRCh38
NC_000013.10:g.113772751A>G , CM000675.1:g.113772751A>G	GRCh37
NC_000013.9:g.112820752A>G	NCBI36
NG_009258.1:g.639A>G , LRG_548:g.639A>G
NG_009262.1:g.17647A>G , LRG_554:g.17647A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000346342.8:c.764A>G MANE Select	ENSP00000329546.4:p.Asp255Gly
ENST00000346342.7:c.764A>G	ENSP00000329546.3:p.Asp255Gly
ENST00000375581.3:c.830A>G	ENSP00000364731.3:p.Asp277Gly
ENST00000541084.5:c.578A>G	ENSP00000442051.2:p.Asp193Gly
NM_000131.4:c.830A>G , LRG_554t1:c.830A>G	NP_000122.1:p.Asp277Gly
NM_001267554.1:c.578A>G	NP_001254483.1:p.Asp193Gly
NM_019616.3:c.764A>G , LRG_554t2:c.764A>G	NP_062562.1:p.Asp255Gly
NR_051961.1:n.851A>G
XM_006719963.2:c.623A>G	XP_006720026.1:p.Asp208Gly
XM_011537474.1:c.872A>G	XP_011535776.1:p.Asp291Gly
XM_011537475.1:c.686A>G	XP_011535777.1:p.Asp229Gly
XM_011537476.1:c.524A>G	XP_011535778.1:p.Asp175Gly
XM_011537477.1:c.833A>G	XP_011535779.1:p.Asp278Gly
XM_006719963.3:c.668A>G	XP_006720026.2:p.Asp223Gly
XM_011537474.2:c.917A>G	XP_011535776.2:p.Asp306Gly
XM_011537475.2:c.731A>G	XP_011535777.2:p.Asp244Gly
XM_011537476.2:c.524A>G	XP_011535778.1:p.Asp175Gly
NM_019616.4:c.764A>G MANE Select	NP_062562.1:p.Asp255Gly
NR_051961.2:n.848A>G
NM_001267554.2:c.578A>G	NP_001254483.1:p.Asp193Gly