Canonical Allele Identifier: CA256458077

Gene: F7

Linked Data

• dbSNP Id: rs138452052
• gnomAD v2: 13-113768011-G-A
• gnomAD v3: 13-113113697-G-A
• gnomAD v4: 13-113113697-G-A
• MyVariant Identifiers: chr13:g.113768011G>A (hg19) ; chr13:g.113113697G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113113697G>A , CM000675.2:g.113113697G>A	GRCh38
NC_000013.10:g.113768011G>A , CM000675.1:g.113768011G>A	GRCh37
NC_000013.9:g.112816012G>A	NCBI36
NG_009262.1:g.12907G>A , LRG_554:g.12907G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.226-55G>A MANE Select	ENSP00000329546.4:n.226-55G>A
ENST00000346342.7:c.226-55G>A	ENSP00000329546.3:n.226-55G>A
ENST00000375581.3:c.292-55G>A	ENSP00000364731.3:n.292-55G>A
ENST00000444337.1:c.212-78G>A	ENSP00000387669.1:n.212-78G>A
ENST00000473085.1:n.173-55G>A
ENST00000479674.1:n.512-78G>A
ENST00000541084.5:c.65-150G>A	ENSP00000442051.2:n.65-150G>A
NM_000131.4:c.292-55G>A , LRG_554t1:c.292-55G>A	NP_000122.1:n.292-55G>A
NM_001267554.1:c.65-150G>A	NP_001254483.1:n.65-150G>A
NM_019616.3:c.226-55G>A , LRG_554t2:c.226-55G>A	NP_062562.1:n.226-55G>A
NR_051961.1:n.266-78G>A
XM_006719963.2:c.226-55G>A	XP_006720026.1:n.226-55G>A
XM_011537474.1:c.226-55G>A	XP_011535776.1:n.226-55G>A
XM_011537475.1:c.65-150G>A	XP_011535777.1:n.65-150G>A
XM_011537477.1:c.212-150G>A	XP_011535779.1:n.212-150G>A
XM_006719963.3:c.271-55G>A	XP_006720026.2:n.271-55G>A
XM_011537474.2:c.271-55G>A	XP_011535776.2:n.271-55G>A
XM_011537475.2:c.110-150G>A	XP_011535777.2:n.110-150G>A
NM_019616.4:c.226-55G>A MANE Select	NP_062562.1:n.226-55G>A
NR_051961.2:n.263-78G>A
NM_001267554.2:c.65-150G>A	NP_001254483.1:n.65-150G>A