Canonical Allele Identifier: CA388785958

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772824C>G (hg19) ; chr13:g.113118510C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118510C>G , CM000675.2:g.113118510C>G	GRCh38
NC_000013.10:g.113772824C>G , CM000675.1:g.113772824C>G	GRCh37
NC_000013.9:g.112820825C>G	NCBI36
NG_009258.1:g.712C>G , LRG_548:g.712C>G
NG_009262.1:g.17720C>G , LRG_554:g.17720C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.837C>G MANE Select	ENSP00000329546.4:p.His279Gln
ENST00000346342.7:c.837C>G	ENSP00000329546.3:p.His279Gln
ENST00000375581.3:c.903C>G	ENSP00000364731.3:p.His301Gln
ENST00000541084.5:c.651C>G	ENSP00000442051.2:p.His217Gln
NM_000131.4:c.903C>G , LRG_554t1:c.903C>G	NP_000122.1:p.His301Gln
NM_001267554.1:c.651C>G	NP_001254483.1:p.His217Gln
NM_019616.3:c.837C>G , LRG_554t2:c.837C>G	NP_062562.1:p.His279Gln
NR_051961.1:n.924C>G
XM_006719963.2:c.696C>G	XP_006720026.1:p.His232Gln
XM_011537474.1:c.945C>G	XP_011535776.1:p.His315Gln
XM_011537475.1:c.759C>G	XP_011535777.1:p.His253Gln
XM_011537476.1:c.597C>G	XP_011535778.1:p.His199Gln
XM_011537477.1:c.906C>G	XP_011535779.1:p.His302Gln
XM_006719963.3:c.741C>G	XP_006720026.2:p.His247Gln
XM_011537474.2:c.990C>G	XP_011535776.2:p.His330Gln
XM_011537475.2:c.804C>G	XP_011535777.2:p.His268Gln
XM_011537476.2:c.597C>G	XP_011535778.1:p.His199Gln
NM_019616.4:c.837C>G MANE Select	NP_062562.1:p.His279Gln
NR_051961.2:n.921C>G
NM_001267554.2:c.651C>G	NP_001254483.1:p.His217Gln