Canonical Allele Identifier: CA1206136205
Gene: F5 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.169530754G= , CM000663.2:g.169530754G= GRCh38
NC_000001.10:g.169499992G= , CM000663.1:g.169499992G= GRCh37
NC_000001.9:g.167766616G= NCBI36
NG_011806.1:g.60778C= , LRG_553:g.60778C=

Transcript Alleles

HGVS Amino-acid change
ENST00000367797.9:c.5208+32C= MANE Select ENSP00000356771.3:n.5208+32C=
ENST00000367796.3:c.5223+32C= ENSP00000356770.3:n.5223+32C=
ENST00000367797.7:c.5208+32C= ENSP00000356771.3:n.5208+32C=
NM_000130.4:c.5208+32C= , LRG_553t1:c.5208+32C= NP_000121.2:n.5208+32C=
XM_017000660.2:c.4797+32C= XP_016856149.1:n.4797+32C=
NM_000130.5:c.5208+32C= MANE Select NP_000121.2:n.5208+32C=
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