Canonical Allele Identifier: CA2466845433
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154957368A= , CM000685.2:g.154957368A= GRCh38
NC_000023.10:g.154185643A= , CM000685.1:g.154185643A= GRCh37
NC_000023.9:g.153838837A= NCBI36
NG_011403.1:g.70356T=
NG_011403.2:g.70356T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1538-197T= MANE Select ENSP00000353393.4:n.1538-197T=
ENST00000647125.1:c.*1414-197T= ENSP00000496062.1:n.*1414-197T=
ENST00000360256.8:c.1538-197T= ENSP00000353393.4:n.1538-197T=
NM_000132.3:c.1538-197T= NP_000123.1:n.1538-197T=
XM_011531126.1:c.1433-197T= XP_011529428.1:n.1433-197T=
NM_000132.4:c.1538-197T= MANE Select NP_000123.1:n.1538-197T=
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