Canonical Allele Identifier: CA2466815599
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863112C= , CM000685.2:g.154863112C= GRCh38
NC_000023.10:g.154091387C= , CM000685.1:g.154091387C= GRCh37
NC_000023.9:g.153744581C= NCBI36
NG_011403.1:g.164612G=
NG_011403.2:g.164612G=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6545G= MANE Select ENSP00000353393.4:p.Arg2182=
ENST00000644698.1:c.278G= ENSP00000495706.1:p.Arg93=
ENST00000330287.10:c.140G= ENSP00000327895.6:p.Arg47=
ENST00000360256.8:c.6545G= ENSP00000353393.4:p.Arg2182=
NM_000132.3:c.6545G= NP_000123.1:p.Arg2182=
NM_019863.2:c.140G= NP_063916.1:p.Arg47=
XM_011531126.1:c.6440G= XP_011529428.1:p.Arg2147=
NM_000132.4:c.6545G= MANE Select NP_000123.1:p.Arg2182=
NM_019863.3:c.140G= NP_063916.1:p.Arg47=