Canonical Allele Identifier: CA2466856585
Gene: F8 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154993181A= , CM000685.2:g.154993181A= GRCh38
NC_000023.10:g.154221456A= , CM000685.1:g.154221456A= GRCh37
NC_000023.9:g.153874650A= NCBI36
NG_011403.1:g.34543T=
NG_011403.2:g.34543T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.389-33T= MANE Select ENSP00000353393.4:n.389-33T=
ENST00000647125.1:c.*175-33T= ENSP00000496062.1:n.*175-33T=
ENST00000360256.8:c.389-33T= ENSP00000353393.4:n.389-33T=
ENST00000423959.5:c.284-33T= ENSP00000409446.1:n.284-33T=
ENST00000453950.1:c.371-33T= ENSP00000389153.1:n.371-33T=
NM_000132.3:c.389-33T= NP_000123.1:n.389-33T=
XM_011531126.1:c.284-33T= XP_011529428.1:n.284-33T=
NM_000132.4:c.389-33T= MANE Select NP_000123.1:n.389-33T=
Search 100 bp 5'
Search 100 bp 3'