Canonical Allele Identifier: CA2466845250
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154956784C= , CM000685.2:g.154956784C= GRCh38
NC_000023.10:g.154185059C= , CM000685.1:g.154185059C= GRCh37
NC_000023.9:g.153838253C= NCBI36
NG_011403.1:g.70940G=
NG_011403.2:g.70940G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1752+173G= MANE Select ENSP00000353393.4:n.1752+173G=
ENST00000647125.1:c.*1628+173G= ENSP00000496062.1:n.*1628+173G=
ENST00000360256.8:c.1752+173G= ENSP00000353393.4:n.1752+173G=
NM_000132.3:c.1752+173G= NP_000123.1:n.1752+173G=
XM_011531126.1:c.1647+173G= XP_011529428.1:n.1647+173G=
NM_000132.4:c.1752+173G= MANE Select NP_000123.1:n.1752+173G=
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