Canonical Allele Identifier: CA2466835685
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928433C= , CM000685.2:g.154928433C= GRCh38
NC_000023.10:g.154156708C= , CM000685.1:g.154156708C= GRCh37
NC_000023.9:g.153809902C= NCBI36
NG_011403.1:g.99291G=
NG_011403.2:g.99291G=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5219+138G= MANE Select ENSP00000353393.4:n.5219+138G=
ENST00000360256.8:c.5219+138G= ENSP00000353393.4:n.5219+138G=
NM_000132.3:c.5219+138G= NP_000123.1:n.5219+138G=
XM_011531126.1:c.5114+138G= XP_011529428.1:n.5114+138G=
NM_000132.4:c.5219+138G= MANE Select NP_000123.1:n.5219+138G=
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