Canonical Allele Identifier: CA2466856685
Gene: F8 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154993487T= , CM000685.2:g.154993487T= GRCh38
NC_000023.10:g.154221762T= , CM000685.1:g.154221762T= GRCh37
NC_000023.9:g.153874956T= NCBI36
NG_011403.1:g.34237A=
NG_011403.2:g.34237A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.389-339A= MANE Select ENSP00000353393.4:n.389-339A=
ENST00000647125.1:c.*175-339A= ENSP00000496062.1:n.*175-339A=
ENST00000360256.8:c.389-339A= ENSP00000353393.4:n.389-339A=
ENST00000423959.5:c.284-339A= ENSP00000409446.1:n.284-339A=
ENST00000453950.1:c.371-339A= ENSP00000389153.1:n.371-339A=
NM_000132.3:c.389-339A= NP_000123.1:n.389-339A=
XM_011531126.1:c.284-339A= XP_011529428.1:n.284-339A=
NM_000132.4:c.389-339A= MANE Select NP_000123.1:n.389-339A=
Search 100 bp 5'
Search 100 bp 3'