Canonical Allele Identifier: CA414906567
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904065T>G , CM000685.2:g.154904065T>G GRCh38
NC_000023.10:g.154132340T>G , CM000685.1:g.154132340T>G GRCh37
NC_000023.9:g.153785534T>G NCBI36
NG_011403.1:g.123659A>C
NG_011403.2:g.123659A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5839A>C MANE Select ENSP00000353393.4:p.Thr1947Pro
ENST00000360256.8:c.5839A>C ENSP00000353393.4:p.Thr1947Pro
NM_000132.3:c.5839A>C NP_000123.1:p.Thr1947Pro
XM_011531126.1:c.5734A>C XP_011529428.1:p.Thr1912Pro
NM_000132.4:c.5839A>C MANE Select NP_000123.1:p.Thr1947Pro