Canonical Allele Identifier: CA414910996
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154953994T>A , CM000685.2:g.154953994T>A GRCh38
NC_000023.10:g.154182269T>A , CM000685.1:g.154182269T>A GRCh37
NC_000023.9:g.153835463T>A NCBI36
NG_011403.1:g.73730A>T
NG_011403.2:g.73730A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1801A>T MANE Select ENSP00000353393.4:p.Asn601Tyr
ENST00000647125.1:c.*1677A>T ENSP00000496062.1:n.*1677A>T
ENST00000360256.8:c.1801A>T ENSP00000353393.4:p.Asn601Tyr
NM_000132.3:c.1801A>T NP_000123.1:p.Asn601Tyr
XM_011531126.1:c.1696A>T XP_011529428.1:p.Asn566Tyr
NM_000132.4:c.1801A>T MANE Select NP_000123.1:p.Asn601Tyr