Canonical Allele Identifier: CA414906672
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904082T>A , CM000685.2:g.154904082T>A GRCh38
NC_000023.10:g.154132357T>A , CM000685.1:g.154132357T>A GRCh37
NC_000023.9:g.153785551T>A NCBI36
NG_011403.1:g.123642A>T
NG_011403.2:g.123642A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5822A>T MANE Select ENSP00000353393.4:p.Asn1941Ile
ENST00000360256.8:c.5822A>T ENSP00000353393.4:p.Asn1941Ile
NM_000132.3:c.5822A>T NP_000123.1:p.Asn1941Ile
XM_011531126.1:c.5717A>T XP_011529428.1:p.Asn1906Ile
NM_000132.4:c.5822A>T MANE Select NP_000123.1:p.Asn1941Ile