Canonical Allele Identifier: CA2466847899
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154965922T= , CM000685.2:g.154965922T= GRCh38
NC_000023.10:g.154194197T= , CM000685.1:g.154194197T= GRCh37
NC_000023.9:g.153847391T= NCBI36
NG_011403.1:g.61802A=
NG_011403.2:g.61802A=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1443+48A= MANE Select ENSP00000353393.4:n.1443+48A=
ENST00000647125.1:c.*1319+48A= ENSP00000496062.1:n.*1319+48A=
ENST00000360256.8:c.1443+48A= ENSP00000353393.4:n.1443+48A=
ENST00000483822.2:n.311A=
NM_000132.3:c.1443+48A= NP_000123.1:n.1443+48A=
XM_011531126.1:c.1338+48A= XP_011529428.1:n.1338+48A=
NM_000132.4:c.1443+48A= MANE Select NP_000123.1:n.1443+48A=
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