Canonical Allele Identifier: CA2466828206
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904104G= , CM000685.2:g.154904104G= GRCh38
NC_000023.10:g.154132379G= , CM000685.1:g.154132379G= GRCh37
NC_000023.9:g.153785573G= NCBI36
NG_011403.1:g.123620C=
NG_011403.2:g.123620C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5816-16C= MANE Select ENSP00000353393.4:n.5816-16C=
ENST00000360256.8:c.5816-16C= ENSP00000353393.4:n.5816-16C=
NM_000132.3:c.5816-16C= NP_000123.1:n.5816-16C=
XM_011531126.1:c.5711-16C= XP_011529428.1:n.5711-16C=
NM_000132.4:c.5816-16C= MANE Select NP_000123.1:n.5816-16C=