Canonical Allele Identifier: CA7060202

Gene: F7

Linked Data

• dbSNP Id: rs768302905
• ExAC: 13:113772966 G / A
• gnomAD v2: 13-113772966-G-A
• gnomAD v3: 13-113118652-G-A
• gnomAD v4: 13-113118652-G-A
• MyVariant Identifiers: chr13:g.113772966G>A (hg19) ; chr13:g.113118652G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118652G>A , CM000675.2:g.113118652G>A	GRCh38
NC_000013.10:g.113772966G>A , CM000675.1:g.113772966G>A	GRCh37
NC_000013.9:g.112820967G>A	NCBI36
NG_009258.1:g.854G>A , LRG_548:g.854G>A
NG_009262.1:g.17862G>A , LRG_554:g.17862G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.979G>A MANE Select	ENSP00000329546.4:p.Asp327Asn
ENST00000346342.7:c.979G>A	ENSP00000329546.3:p.Asp327Asn
ENST00000375581.3:c.1045G>A	ENSP00000364731.3:p.Asp349Asn
ENST00000541084.5:c.793G>A	ENSP00000442051.2:p.Asp265Asn
NM_000131.4:c.1045G>A , LRG_554t1:c.1045G>A	NP_000122.1:p.Asp349Asn
NM_001267554.1:c.793G>A	NP_001254483.1:p.Asp265Asn
NM_019616.3:c.979G>A , LRG_554t2:c.979G>A	NP_062562.1:p.Asp327Asn
NR_051961.1:n.1066G>A
XM_006719963.2:c.838G>A	XP_006720026.1:p.Asp280Asn
XM_011537474.1:c.1087G>A	XP_011535776.1:p.Asp363Asn
XM_011537475.1:c.901G>A	XP_011535777.1:p.Asp301Asn
XM_011537476.1:c.739G>A	XP_011535778.1:p.Asp247Asn
XM_011537477.1:c.1048G>A	XP_011535779.1:p.Asp350Asn
XM_006719963.3:c.883G>A	XP_006720026.2:p.Asp295Asn
XM_011537474.2:c.1132G>A	XP_011535776.2:p.Asp378Asn
XM_011537475.2:c.946G>A	XP_011535777.2:p.Asp316Asn
XM_011537476.2:c.739G>A	XP_011535778.1:p.Asp247Asn
NM_019616.4:c.979G>A MANE Select	NP_062562.1:p.Asp327Asn
NR_051961.2:n.1063G>A
NM_001267554.2:c.793G>A	NP_001254483.1:p.Asp265Asn