Canonical Allele Identifier: CA388786596

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113773101G>C (hg19) ; chr13:g.113118787G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118787G>C , CM000675.2:g.113118787G>C	GRCh38
NC_000013.10:g.113773101G>C , CM000675.1:g.113773101G>C	GRCh37
NC_000013.9:g.112821102G>C	NCBI36
NG_009258.1:g.989G>C , LRG_548:g.989G>C
NG_009262.1:g.17997G>C , LRG_554:g.17997G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.1114G>C MANE Select	ENSP00000329546.4:p.Asp372His
ENST00000346342.7:c.1114G>C	ENSP00000329546.3:p.Asp372His
ENST00000375581.3:c.1180G>C	ENSP00000364731.3:p.Asp394His
ENST00000541084.5:c.928G>C	ENSP00000442051.2:p.Asp310His
NM_000131.4:c.1180G>C , LRG_554t1:c.1180G>C	NP_000122.1:p.Asp394His
NM_001267554.1:c.928G>C	NP_001254483.1:p.Asp310His
NM_019616.3:c.1114G>C , LRG_554t2:c.1114G>C	NP_062562.1:p.Asp372His
NR_051961.1:n.1201G>C
XM_006719963.2:c.973G>C	XP_006720026.1:p.Asp325His
XM_011537474.1:c.1222G>C	XP_011535776.1:p.Asp408His
XM_011537475.1:c.1036G>C	XP_011535777.1:p.Asp346His
XM_011537476.1:c.874G>C	XP_011535778.1:p.Asp292His
XM_011537477.1:c.1183G>C	XP_011535779.1:p.Asp395His
XM_006719963.3:c.1018G>C	XP_006720026.2:p.Asp340His
XM_011537474.2:c.1267G>C	XP_011535776.2:p.Asp423His
XM_011537475.2:c.1081G>C	XP_011535777.2:p.Asp361His
XM_011537476.2:c.874G>C	XP_011535778.1:p.Asp292His
NM_019616.4:c.1114G>C MANE Select	NP_062562.1:p.Asp372His
NR_051961.2:n.1198G>C
NM_001267554.2:c.928G>C	NP_001254483.1:p.Asp310His