Canonical Allele Identifier: CA2466807403
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837578G= , CM000685.2:g.154837578G= GRCh38
NC_000023.10:g.154065853G= , CM000685.1:g.154065853G= GRCh37
NC_000023.9:g.153719047G= NCBI36
NG_011403.1:g.190146C=
NG_033065.1:g.2085C=
NG_011403.2:g.190146C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.*19C= MANE Select ENSP00000353393.4:n.*19C=
ENST00000644698.1:c.*19C= ENSP00000495706.1:n.*19C=
ENST00000330287.10:c.*19C= ENSP00000327895.6:n.*19C=
ENST00000360256.8:c.*19C= ENSP00000353393.4:n.*19C=
NM_000132.3:c.*19C= NP_000123.1:n.*19C=
NM_019863.2:c.*19C= NP_063916.1:n.*19C=
XM_011531126.1:c.*19C= XP_011529428.1:n.*19C=
NM_000132.4:c.*19C= MANE Select NP_000123.1:n.*19C=
NM_019863.3:c.*19C= NP_063916.1:n.*19C=