Canonical Allele Identifier: CA414920017
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997041A>T , CM000685.2:g.154997041A>T GRCh38
NC_000023.10:g.154225316A>T , CM000685.1:g.154225316A>T GRCh37
NC_000023.9:g.153878510A>T NCBI36
NG_011403.1:g.30683T>A
NG_011403.2:g.30683T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.320T>A MANE Select ENSP00000353393.4:p.Leu107His
ENST00000647125.1:c.*106T>A ENSP00000496062.1:n.*106T>A
ENST00000360256.8:c.320T>A ENSP00000353393.4:p.Leu107His
ENST00000423959.5:c.215T>A ENSP00000409446.1:p.Leu72His
ENST00000453950.1:c.302T>A ENSP00000389153.1:p.Leu101His
NM_000132.3:c.320T>A NP_000123.1:p.Leu107His
XM_011531126.1:c.215T>A XP_011529428.1:p.Leu72His
NM_000132.4:c.320T>A MANE Select NP_000123.1:p.Leu107His