Canonical Allele Identifier: CA388786836

Gene: F7

Linked Data

• dbSNP Id: rs2036248120
• MyVariant Identifiers: chr13:g.113773153A>G (hg19) ; chr13:g.113118839A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118839A>G , CM000675.2:g.113118839A>G	GRCh38
NC_000013.10:g.113773153A>G , CM000675.1:g.113773153A>G	GRCh37
NC_000013.9:g.112821154A>G	NCBI36
NG_009258.1:g.1041A>G , LRG_548:g.1041A>G
NG_009262.1:g.18049A>G , LRG_554:g.18049A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1166A>G MANE Select	ENSP00000329546.4:p.His389Arg
ENST00000346342.7:c.1166A>G	ENSP00000329546.3:p.His389Arg
ENST00000375581.3:c.1232A>G	ENSP00000364731.3:p.His411Arg
ENST00000541084.5:c.980A>G	ENSP00000442051.2:p.His327Arg
NM_000131.4:c.1232A>G , LRG_554t1:c.1232A>G	NP_000122.1:p.His411Arg
NM_001267554.1:c.980A>G	NP_001254483.1:p.His327Arg
NM_019616.3:c.1166A>G , LRG_554t2:c.1166A>G	NP_062562.1:p.His389Arg
NR_051961.1:n.1253A>G
XM_006719963.2:c.1025A>G	XP_006720026.1:p.His342Arg
XM_011537474.1:c.1274A>G	XP_011535776.1:p.His425Arg
XM_011537475.1:c.1088A>G	XP_011535777.1:p.His363Arg
XM_011537476.1:c.926A>G	XP_011535778.1:p.His309Arg
XM_011537477.1:c.1235A>G	XP_011535779.1:p.His412Arg
XM_006719963.3:c.1070A>G	XP_006720026.2:p.His357Arg
XM_011537474.2:c.1319A>G	XP_011535776.2:p.His440Arg
XM_011537475.2:c.1133A>G	XP_011535777.2:p.His378Arg
XM_011537476.2:c.926A>G	XP_011535778.1:p.His309Arg
NM_019616.4:c.1166A>G MANE Select	NP_062562.1:p.His389Arg
NR_051961.2:n.1250A>G
NM_001267554.2:c.980A>G	NP_001254483.1:p.His327Arg