Canonical Allele Identifier: CA414920100
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997078T>G , CM000685.2:g.154997078T>G GRCh38
NC_000023.10:g.154225353T>G , CM000685.1:g.154225353T>G GRCh37
NC_000023.9:g.153878547T>G NCBI36
NG_011403.1:g.30646A>C
NG_011403.2:g.30646A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.283A>C MANE Select ENSP00000353393.4:p.Ile95Leu
ENST00000647125.1:c.*69A>C ENSP00000496062.1:n.*69A>C
ENST00000360256.8:c.283A>C ENSP00000353393.4:p.Ile95Leu
ENST00000423959.5:c.178A>C ENSP00000409446.1:p.Ile60Leu
ENST00000453950.1:c.265A>C ENSP00000389153.1:p.Ile89Leu
NM_000132.3:c.283A>C NP_000123.1:p.Ile95Leu
XM_011531126.1:c.178A>C XP_011529428.1:p.Ile60Leu
NM_000132.4:c.283A>C MANE Select NP_000123.1:p.Ile95Leu