Canonical Allele Identifier: CA7060221

Gene: F7

Linked Data

• dbSNP Id: rs769374785
• ExAC: 13:113773025 G / A
• gnomAD v2: 13-113773025-G-A
• gnomAD v3: 13-113118711-G-A
• gnomAD v4: 13-113118711-G-A
• MyVariant Identifiers: chr13:g.113773025G>A (hg19) ; chr13:g.113118711G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118711G>A , CM000675.2:g.113118711G>A	GRCh38
NC_000013.10:g.113773025G>A , CM000675.1:g.113773025G>A	GRCh37
NC_000013.9:g.112821026G>A	NCBI36
NG_009258.1:g.913G>A , LRG_548:g.913G>A
NG_009262.1:g.17921G>A , LRG_554:g.17921G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1038G>A MANE Select	ENSP00000329546.4:p.Gln346=
ENST00000346342.7:c.1038G>A	ENSP00000329546.3:p.Gln346=
ENST00000375581.3:c.1104G>A	ENSP00000364731.3:p.Gln368=
ENST00000541084.5:c.852G>A	ENSP00000442051.2:p.Gln284=
NM_000131.4:c.1104G>A , LRG_554t1:c.1104G>A	NP_000122.1:p.Gln368=
NM_001267554.1:c.852G>A	NP_001254483.1:p.Gln284=
NM_019616.3:c.1038G>A , LRG_554t2:c.1038G>A	NP_062562.1:p.Gln346=
NR_051961.1:n.1125G>A
XM_006719963.2:c.897G>A	XP_006720026.1:p.Gln299=
XM_011537474.1:c.1146G>A	XP_011535776.1:p.Gln382=
XM_011537475.1:c.960G>A	XP_011535777.1:p.Gln320=
XM_011537476.1:c.798G>A	XP_011535778.1:p.Gln266=
XM_011537477.1:c.1107G>A	XP_011535779.1:p.Gln369=
XM_006719963.3:c.942G>A	XP_006720026.2:p.Gln314=
XM_011537474.2:c.1191G>A	XP_011535776.2:p.Gln397=
XM_011537475.2:c.1005G>A	XP_011535777.2:p.Gln335=
XM_011537476.2:c.798G>A	XP_011535778.1:p.Gln266=
NM_019616.4:c.1038G>A MANE Select	NP_062562.1:p.Gln346=
NR_051961.2:n.1122G>A
NM_001267554.2:c.852G>A	NP_001254483.1:p.Gln284=