Canonical Allele Identifier: CA2466828163
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903993T= , CM000685.2:g.154903993T= GRCh38
NC_000023.10:g.154132268T= , CM000685.1:g.154132268T= GRCh37
NC_000023.9:g.153785462T= NCBI36
NG_011403.1:g.123731A=
NG_011403.2:g.123731A=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5911A= MANE Select ENSP00000353393.4:p.Asn1971=
ENST00000360256.8:c.5911A= ENSP00000353393.4:p.Asn1971=
NM_000132.3:c.5911A= NP_000123.1:p.Asn1971=
XM_011531126.1:c.5806A= XP_011529428.1:p.Asn1936=
NM_000132.4:c.5911A= MANE Select NP_000123.1:p.Asn1971=