Canonical Allele Identifier: CA414905900
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903974A>G , CM000685.2:g.154903974A>G GRCh38
NC_000023.10:g.154132249A>G , CM000685.1:g.154132249A>G GRCh37
NC_000023.9:g.153785443A>G NCBI36
NG_011403.1:g.123750T>C
NG_011403.2:g.123750T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5930T>C MANE Select ENSP00000353393.4:p.Phe1977Ser
ENST00000360256.8:c.5930T>C ENSP00000353393.4:p.Phe1977Ser
NM_000132.3:c.5930T>C NP_000123.1:p.Phe1977Ser
XM_011531126.1:c.5825T>C XP_011529428.1:p.Phe1942Ser
NM_000132.4:c.5930T>C MANE Select NP_000123.1:p.Phe1977Ser