Canonical Allele Identifier: CA2466857827
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1603436664

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997173A>G , CM000685.2:g.154997173A>G GRCh38
NC_000023.10:g.154225448A>G , CM000685.1:g.154225448A>G GRCh37
NC_000023.9:g.153878642A>G NCBI36
NG_011403.1:g.30551T>C
NG_011403.2:g.30551T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.266-78T>C MANE Select ENSP00000353393.4:n.266-78T>C
ENST00000647125.1:c.*52-78T>C ENSP00000496062.1:n.*52-78T>C
ENST00000360256.8:c.266-78T>C ENSP00000353393.4:n.266-78T>C
ENST00000423959.5:c.161-78T>C ENSP00000409446.1:n.161-78T>C
ENST00000453950.1:c.248-78T>C ENSP00000389153.1:n.248-78T>C
NM_000132.3:c.266-78T>C NP_000123.1:n.266-78T>C
XM_011531126.1:c.161-78T>C XP_011529428.1:n.161-78T>C
NM_000132.4:c.266-78T>C MANE Select NP_000123.1:n.266-78T>C