Canonical Allele Identifier: CA2466807327
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837397G= , CM000685.2:g.154837397G= GRCh38
NC_000023.10:g.154065672G= , CM000685.1:g.154065672G= GRCh37
NC_000023.9:g.153718866G= NCBI36
NG_011403.1:g.190327C=
NG_033065.1:g.2266C=
NG_011403.2:g.190327C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.*200C= MANE Select ENSP00000353393.4:n.*200C=
ENST00000644698.1:c.*200C= ENSP00000495706.1:n.*200C=
ENST00000330287.10:c.*200C= ENSP00000327895.6:n.*200C=
ENST00000360256.8:c.*200C= ENSP00000353393.4:n.*200C=
NM_000132.3:c.*200C= NP_000123.1:n.*200C=
NM_019863.2:c.*200C= NP_063916.1:n.*200C=
XM_011531126.1:c.*200C= XP_011529428.1:n.*200C=
NM_000132.4:c.*200C= MANE Select NP_000123.1:n.*200C=
NM_019863.3:c.*200C= NP_063916.1:n.*200C=