Canonical Allele Identifier: CA2466845283
Gene: F8 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154956873A= , CM000685.2:g.154956873A= GRCh38
NC_000023.10:g.154185148A= , CM000685.1:g.154185148A= GRCh37
NC_000023.9:g.153838342A= NCBI36
NG_011403.1:g.70851T=
NG_011403.2:g.70851T=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1752+84T= MANE Select ENSP00000353393.4:n.1752+84T=
ENST00000647125.1:c.*1628+84T= ENSP00000496062.1:n.*1628+84T=
ENST00000360256.8:c.1752+84T= ENSP00000353393.4:n.1752+84T=
NM_000132.3:c.1752+84T= NP_000123.1:n.1752+84T=
XM_011531126.1:c.1647+84T= XP_011529428.1:n.1647+84T=
NM_000132.4:c.1752+84T= MANE Select NP_000123.1:n.1752+84T=
Search 100 bp 5'
Search 100 bp 3'