Canonical Allele Identifier: CA414905807
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903964A>C , CM000685.2:g.154903964A>C GRCh38
NC_000023.10:g.154132239A>C , CM000685.1:g.154132239A>C GRCh37
NC_000023.9:g.153785433A>C NCBI36
NG_011403.1:g.123760T>G
NG_011403.2:g.123760T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5940T>G MANE Select ENSP00000353393.4:p.His1980Gln
ENST00000360256.8:c.5940T>G ENSP00000353393.4:p.His1980Gln
NM_000132.3:c.5940T>G NP_000123.1:p.His1980Gln
XM_011531126.1:c.5835T>G XP_011529428.1:p.His1945Gln
NM_000132.4:c.5940T>G MANE Select NP_000123.1:p.His1980Gln