Canonical Allele Identifier: CA414903468
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154860490A>T , CM000685.2:g.154860490A>T GRCh38
NC_000023.10:g.154088765A>T , CM000685.1:g.154088765A>T GRCh37
NC_000023.9:g.153741959A>T NCBI36
NG_011403.1:g.167234T>A
NG_011403.2:g.167234T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6842T>A MANE Select ENSP00000353393.4:p.Ile2281Asn
ENST00000644698.1:c.575T>A ENSP00000495706.1:p.Ile192Asn
ENST00000330287.10:c.437T>A ENSP00000327895.6:p.Ile146Asn
ENST00000360256.8:c.6842T>A ENSP00000353393.4:p.Ile2281Asn
NM_000132.3:c.6842T>A NP_000123.1:p.Ile2281Asn
NM_019863.2:c.437T>A NP_063916.1:p.Ile146Asn
XM_011531126.1:c.6737T>A XP_011529428.1:p.Ile2246Asn
NM_000132.4:c.6842T>A MANE Select NP_000123.1:p.Ile2281Asn
NM_019863.3:c.437T>A NP_063916.1:p.Ile146Asn