Canonical Allele Identifier: CA414919915
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154996994A>T , CM000685.2:g.154996994A>T GRCh38
NC_000023.10:g.154225269A>T , CM000685.1:g.154225269A>T GRCh37
NC_000023.9:g.153878463A>T NCBI36
NG_011403.1:g.30730T>A
NG_011403.2:g.30730T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.367T>A MANE Select ENSP00000353393.4:p.Ser123Thr
ENST00000647125.1:c.*153T>A ENSP00000496062.1:n.*153T>A
ENST00000360256.8:c.367T>A ENSP00000353393.4:p.Ser123Thr
ENST00000423959.5:c.262T>A ENSP00000409446.1:p.Ser88Thr
ENST00000453950.1:c.349T>A ENSP00000389153.1:p.Ser117Thr
NM_000132.3:c.367T>A NP_000123.1:p.Ser123Thr
XM_011531126.1:c.262T>A XP_011529428.1:p.Ser88Thr
NM_000132.4:c.367T>A MANE Select NP_000123.1:p.Ser123Thr