Canonical Allele Identifier: CA890929627
Gene: F5 HGNC NCBI

Linked Data

dbSNP Id: rs1231770639
MyVariant Identifiers: chr1:g.169524095del (hg19) chr1:g.169554857del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169554859del , CM000663.2:g.169554859del GRCh38
NC_000001.10:g.169524097del , CM000663.1:g.169524097del GRCh37
NC_000001.9:g.167790721del NCBI36
NG_011806.1:g.36675del , LRG_553:g.36675del

Transcript Alleles

HGVS Amino-acid Change
ENST00000367797.9:c.1118+325del MANE Select ENSP00000356771.3:n.1118+325del
ENST00000367796.3:c.1118+325del ENSP00000356770.3:n.1118+325del
ENST00000367797.7:c.1118+325del ENSP00000356771.3:n.1118+325del
NM_000130.4:c.1118+325del , LRG_553t1:c.1118+325del NP_000121.2:n.1118+325del
XM_017000660.2:c.707+325del XP_016856149.1:n.707+325del
NM_000130.5:c.1118+325del MANE Select NP_000121.2:n.1118+325del
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