Canonical Allele Identifier: CA2466815596
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863111G= , CM000685.2:g.154863111G= GRCh38
NC_000023.10:g.154091386G= , CM000685.1:g.154091386G= GRCh37
NC_000023.9:g.153744580G= NCBI36
NG_011403.1:g.164613C=
NG_011403.2:g.164613C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6546C= MANE Select ENSP00000353393.4:p.Arg2182=
ENST00000644698.1:c.279C= ENSP00000495706.1:p.Arg93=
ENST00000330287.10:c.141C= ENSP00000327895.6:p.Arg47=
ENST00000360256.8:c.6546C= ENSP00000353393.4:p.Arg2182=
NM_000132.3:c.6546C= NP_000123.1:p.Arg2182=
NM_019863.2:c.141C= NP_063916.1:p.Arg47=
XM_011531126.1:c.6441C= XP_011529428.1:p.Arg2147=
NM_000132.4:c.6546C= MANE Select NP_000123.1:p.Arg2182=
NM_019863.3:c.141C= NP_063916.1:p.Arg47=