Canonical Allele Identifier: CA414917767
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969382T>C , CM000685.2:g.154969382T>C GRCh38
NC_000023.10:g.154197657T>C , CM000685.1:g.154197657T>C GRCh37
NC_000023.9:g.153850851T>C NCBI36
NG_011403.1:g.58342A>G
NG_011403.2:g.58342A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.958A>G MANE Select ENSP00000353393.4:p.Met320Val
ENST00000647125.1:c.*834A>G ENSP00000496062.1:n.*834A>G
ENST00000360256.8:c.958A>G ENSP00000353393.4:p.Met320Val
NM_000132.3:c.958A>G NP_000123.1:p.Met320Val
XM_011531126.1:c.853A>G XP_011529428.1:p.Met285Val
NM_000132.4:c.958A>G MANE Select NP_000123.1:p.Met320Val