Canonical Allele Identifier: CA414910736
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154953955G>T , CM000685.2:g.154953955G>T GRCh38
NC_000023.10:g.154182230G>T , CM000685.1:g.154182230G>T GRCh37
NC_000023.9:g.153835424G>T NCBI36
NG_011403.1:g.73769C>A
NG_011403.2:g.73769C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1840C>A MANE Select ENSP00000353393.4:p.Leu614Ile
ENST00000647125.1:c.*1716C>A ENSP00000496062.1:n.*1716C>A
ENST00000360256.8:c.1840C>A ENSP00000353393.4:p.Leu614Ile
NM_000132.3:c.1840C>A NP_000123.1:p.Leu614Ile
XM_011531126.1:c.1735C>A XP_011529428.1:p.Leu579Ile
NM_000132.4:c.1840C>A MANE Select NP_000123.1:p.Leu614Ile