Canonical Allele Identifier: CA2466845289
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154956914A= , CM000685.2:g.154956914A= GRCh38
NC_000023.10:g.154185189A= , CM000685.1:g.154185189A= GRCh37
NC_000023.9:g.153838383A= NCBI36
NG_011403.1:g.70810T=
NG_011403.2:g.70810T=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1752+43T= MANE Select ENSP00000353393.4:n.1752+43T=
ENST00000647125.1:c.*1628+43T= ENSP00000496062.1:n.*1628+43T=
ENST00000360256.8:c.1752+43T= ENSP00000353393.4:n.1752+43T=
NM_000132.3:c.1752+43T= NP_000123.1:n.1752+43T=
XM_011531126.1:c.1647+43T= XP_011529428.1:n.1647+43T=
NM_000132.4:c.1752+43T= MANE Select NP_000123.1:n.1752+43T=
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