Canonical Allele Identifier: CA414902950
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154860444A>T , CM000685.2:g.154860444A>T GRCh38
NC_000023.10:g.154088719A>T , CM000685.1:g.154088719A>T GRCh37
NC_000023.9:g.153741913A>T NCBI36
NG_011403.1:g.167280T>A
NG_011403.2:g.167280T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6888T>A MANE Select ENSP00000353393.4:p.Asn2296Lys
ENST00000644698.1:c.621T>A ENSP00000495706.1:p.Asn207Lys
ENST00000330287.10:c.483T>A ENSP00000327895.6:p.Asn161Lys
ENST00000360256.8:c.6888T>A ENSP00000353393.4:p.Asn2296Lys
NM_000132.3:c.6888T>A NP_000123.1:p.Asn2296Lys
NM_019863.2:c.483T>A NP_063916.1:p.Asn161Lys
XM_011531126.1:c.6783T>A XP_011529428.1:p.Asn2261Lys
NM_000132.4:c.6888T>A MANE Select NP_000123.1:p.Asn2296Lys
NM_019863.3:c.483T>A NP_063916.1:p.Asn161Lys