Canonical Allele Identifier: CA2466857822
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997132G= , CM000685.2:g.154997132G= GRCh38
NC_000023.10:g.154225407G= , CM000685.1:g.154225407G= GRCh37
NC_000023.9:g.153878601G= NCBI36
NG_011403.1:g.30592C=
NG_011403.2:g.30592C=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.266-37C= MANE Select ENSP00000353393.4:n.266-37C=
ENST00000647125.1:c.*52-37C= ENSP00000496062.1:n.*52-37C=
ENST00000360256.8:c.266-37C= ENSP00000353393.4:n.266-37C=
ENST00000423959.5:c.161-37C= ENSP00000409446.1:n.161-37C=
ENST00000453950.1:c.248-37C= ENSP00000389153.1:n.248-37C=
NM_000132.3:c.266-37C= NP_000123.1:n.266-37C=
XM_011531126.1:c.161-37C= XP_011529428.1:n.161-37C=
NM_000132.4:c.266-37C= MANE Select NP_000123.1:n.266-37C=