Canonical Allele Identifier: CA388785944

Gene: F7

Linked Data

• MyVariant Identifiers: chr13:g.113772819A>C (hg19) ; chr13:g.113118505A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.113118505A>C , CM000675.2:g.113118505A>C	GRCh38
NC_000013.10:g.113772819A>C , CM000675.1:g.113772819A>C	GRCh37
NC_000013.9:g.112820820A>C	NCBI36
NG_009258.1:g.707A>C , LRG_548:g.707A>C
NG_009262.1:g.17715A>C , LRG_554:g.17715A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000346342.8:c.832A>C MANE Select	ENSP00000329546.4:p.Asn278His
ENST00000346342.7:c.832A>C	ENSP00000329546.3:p.Asn278His
ENST00000375581.3:c.898A>C	ENSP00000364731.3:p.Asn300His
ENST00000541084.5:c.646A>C	ENSP00000442051.2:p.Asn216His
NM_000131.4:c.898A>C , LRG_554t1:c.898A>C	NP_000122.1:p.Asn300His
NM_001267554.1:c.646A>C	NP_001254483.1:p.Asn216His
NM_019616.3:c.832A>C , LRG_554t2:c.832A>C	NP_062562.1:p.Asn278His
NR_051961.1:n.919A>C
XM_006719963.2:c.691A>C	XP_006720026.1:p.Asn231His
XM_011537474.1:c.940A>C	XP_011535776.1:p.Asn314His
XM_011537475.1:c.754A>C	XP_011535777.1:p.Asn252His
XM_011537476.1:c.592A>C	XP_011535778.1:p.Asn198His
XM_011537477.1:c.901A>C	XP_011535779.1:p.Asn301His
XM_006719963.3:c.736A>C	XP_006720026.2:p.Asn246His
XM_011537474.2:c.985A>C	XP_011535776.2:p.Asn329His
XM_011537475.2:c.799A>C	XP_011535777.2:p.Asn267His
XM_011537476.2:c.592A>C	XP_011535778.1:p.Asn198His
NM_019616.4:c.832A>C MANE Select	NP_062562.1:p.Asn278His
NR_051961.2:n.916A>C
NM_001267554.2:c.646A>C	NP_001254483.1:p.Asn216His