Canonical Allele Identifier: CA2466846443
Gene: F8 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154960978T= , CM000685.2:g.154960978T= GRCh38
NC_000023.10:g.154189253T= , CM000685.1:g.154189253T= GRCh37
NC_000023.9:g.153842447T= NCBI36
NG_011403.1:g.66746A=
NG_011403.2:g.66746A=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1537+97A= MANE Select ENSP00000353393.4:n.1537+97A=
ENST00000647125.1:c.*1413+97A= ENSP00000496062.1:n.*1413+97A=
ENST00000360256.8:c.1537+97A= ENSP00000353393.4:n.1537+97A=
NM_000132.3:c.1537+97A= NP_000123.1:n.1537+97A=
XM_011531126.1:c.1432+97A= XP_011529428.1:n.1432+97A=
NM_000132.4:c.1537+97A= MANE Select NP_000123.1:n.1537+97A=
Search 100 bp 5'
Search 100 bp 3'