Canonical Allele Identifier: CA414919997
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997032A>G , CM000685.2:g.154997032A>G GRCh38
NC_000023.10:g.154225307A>G , CM000685.1:g.154225307A>G GRCh37
NC_000023.9:g.153878501A>G NCBI36
NG_011403.1:g.30692T>C
NG_011403.2:g.30692T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.329T>C MANE Select ENSP00000353393.4:p.Met110Thr
ENST00000647125.1:c.*115T>C ENSP00000496062.1:n.*115T>C
ENST00000360256.8:c.329T>C ENSP00000353393.4:p.Met110Thr
ENST00000423959.5:c.224T>C ENSP00000409446.1:p.Met75Thr
ENST00000453950.1:c.311T>C ENSP00000389153.1:p.Met104Thr
NM_000132.3:c.329T>C NP_000123.1:p.Met110Thr
XM_011531126.1:c.224T>C XP_011529428.1:p.Met75Thr
NM_000132.4:c.329T>C MANE Select NP_000123.1:p.Met110Thr