Canonical Allele Identifier: CA414905991
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154903987G>T , CM000685.2:g.154903987G>T GRCh38
NC_000023.10:g.154132262G>T , CM000685.1:g.154132262G>T GRCh37
NC_000023.9:g.153785456G>T NCBI36
NG_011403.1:g.123737C>A
NG_011403.2:g.123737C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5917C>A MANE Select ENSP00000353393.4:p.His1973Asn
ENST00000360256.8:c.5917C>A ENSP00000353393.4:p.His1973Asn
NM_000132.3:c.5917C>A NP_000123.1:p.His1973Asn
XM_011531126.1:c.5812C>A XP_011529428.1:p.His1938Asn
NM_000132.4:c.5917C>A MANE Select NP_000123.1:p.His1973Asn