Canonical Allele Identifier: CA414906051
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903997A>T , CM000685.2:g.154903997A>T GRCh38
NC_000023.10:g.154132272A>T , CM000685.1:g.154132272A>T GRCh37
NC_000023.9:g.153785466A>T NCBI36
NG_011403.1:g.123727T>A
NG_011403.2:g.123727T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5907T>A MANE Select ENSP00000353393.4:p.Asn1969Lys
ENST00000360256.8:c.5907T>A ENSP00000353393.4:p.Asn1969Lys
NM_000132.3:c.5907T>A NP_000123.1:p.Asn1969Lys
XM_011531126.1:c.5802T>A XP_011529428.1:p.Asn1934Lys
NM_000132.4:c.5907T>A MANE Select NP_000123.1:p.Asn1969Lys