Canonical Allele Identifier: CA414905469
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903917T>A , CM000685.2:g.154903917T>A GRCh38
NC_000023.10:g.154132192T>A , CM000685.1:g.154132192T>A GRCh37
NC_000023.9:g.153785386T>A NCBI36
NG_011403.1:g.123807A>T
NG_011403.2:g.123807A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5987A>T MANE Select ENSP00000353393.4:p.Asn1996Ile
ENST00000360256.8:c.5987A>T ENSP00000353393.4:p.Asn1996Ile
NM_000132.3:c.5987A>T NP_000123.1:p.Asn1996Ile
XM_011531126.1:c.5882A>T XP_011529428.1:p.Asn1961Ile
NM_000132.4:c.5987A>T MANE Select NP_000123.1:p.Asn1996Ile