Canonical Allele Identifier: CA2466807505
Gene: F8 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837858A= , CM000685.2:g.154837858A= GRCh38
NC_000023.10:g.154066133A= , CM000685.1:g.154066133A= GRCh37
NC_000023.9:g.153719327A= NCBI36
NG_011403.1:g.189866T=
NG_033065.1:g.1805T=
NG_011403.2:g.189866T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6901-106T= MANE Select ENSP00000353393.4:n.6901-106T=
ENST00000644698.1:c.634-106T= ENSP00000495706.1:n.634-106T=
ENST00000330287.10:c.496-106T= ENSP00000327895.6:n.496-106T=
ENST00000360256.8:c.6901-106T= ENSP00000353393.4:n.6901-106T=
NM_000132.3:c.6901-106T= NP_000123.1:n.6901-106T=
NM_019863.2:c.496-106T= NP_063916.1:n.496-106T=
XM_011531126.1:c.6796-106T= XP_011529428.1:n.6796-106T=
NM_000132.4:c.6901-106T= MANE Select NP_000123.1:n.6901-106T=
NM_019863.3:c.496-106T= NP_063916.1:n.496-106T=
Search 100 bp 5'
Search 100 bp 3'