Canonical Allele Identifier: CA388785953

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772822C>G (hg19) ; chr13:g.113118508C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118508C>G , CM000675.2:g.113118508C>G	GRCh38
NC_000013.10:g.113772822C>G , CM000675.1:g.113772822C>G	GRCh37
NC_000013.9:g.112820823C>G	NCBI36
NG_009258.1:g.710C>G , LRG_548:g.710C>G
NG_009262.1:g.17718C>G , LRG_554:g.17718C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.835C>G MANE Select	ENSP00000329546.4:p.His279Asp
ENST00000346342.7:c.835C>G	ENSP00000329546.3:p.His279Asp
ENST00000375581.3:c.901C>G	ENSP00000364731.3:p.His301Asp
ENST00000541084.5:c.649C>G	ENSP00000442051.2:p.His217Asp
NM_000131.4:c.901C>G , LRG_554t1:c.901C>G	NP_000122.1:p.His301Asp
NM_001267554.1:c.649C>G	NP_001254483.1:p.His217Asp
NM_019616.3:c.835C>G , LRG_554t2:c.835C>G	NP_062562.1:p.His279Asp
NR_051961.1:n.922C>G
XM_006719963.2:c.694C>G	XP_006720026.1:p.His232Asp
XM_011537474.1:c.943C>G	XP_011535776.1:p.His315Asp
XM_011537475.1:c.757C>G	XP_011535777.1:p.His253Asp
XM_011537476.1:c.595C>G	XP_011535778.1:p.His199Asp
XM_011537477.1:c.904C>G	XP_011535779.1:p.His302Asp
XM_006719963.3:c.739C>G	XP_006720026.2:p.His247Asp
XM_011537474.2:c.988C>G	XP_011535776.2:p.His330Asp
XM_011537475.2:c.802C>G	XP_011535777.2:p.His268Asp
XM_011537476.2:c.595C>G	XP_011535778.1:p.His199Asp
NM_019616.4:c.835C>G MANE Select	NP_062562.1:p.His279Asp
NR_051961.2:n.919C>G
NM_001267554.2:c.649C>G	NP_001254483.1:p.His217Asp