Canonical Allele Identifier: CA414900114
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896193T>G , CM000685.2:g.154896193T>G GRCh38
NC_000023.10:g.154124468T>G , CM000685.1:g.154124468T>G GRCh37
NC_000023.9:g.153777662T>G NCBI36
NG_011403.1:g.131531A>C
NG_011403.2:g.131531A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6313A>C MANE Select ENSP00000353393.4:p.Thr2105Pro
ENST00000360256.8:c.6313A>C ENSP00000353393.4:p.Thr2105Pro
NM_000132.3:c.6313A>C NP_000123.1:p.Thr2105Pro
XM_011531126.1:c.6208A>C XP_011529428.1:p.Thr2070Pro
NM_000132.4:c.6313A>C MANE Select NP_000123.1:p.Thr2105Pro