Canonical Allele Identifier: CA414920686
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022525A>T , CM000685.2:g.155022525A>T GRCh38
NC_000023.10:g.154250800A>T , CM000685.1:g.154250800A>T GRCh37
NC_000023.9:g.153903994A>T NCBI36
NG_011403.1:g.5199T>A
NG_011403.2:g.5199T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.28T>A MANE Select ENSP00000353393.4:p.Phe10Ile
ENST00000647125.1:c.28T>A ENSP00000496062.1:p.Phe10Ile
ENST00000360256.8:c.28T>A ENSP00000353393.4:p.Phe10Ile
ENST00000423959.5:c.38+4255T>A ENSP00000409446.1:n.38+4255T>A
ENST00000453950.1:c.39-29T>A ENSP00000389153.1:n.39-29T>A
NM_000132.3:c.28T>A NP_000123.1:p.Phe10Ile
XM_011531126.1:c.38+4255T>A XP_011529428.1:n.38+4255T>A
NM_000132.4:c.28T>A MANE Select NP_000123.1:p.Phe10Ile