Canonical Allele Identifier: CA414914678
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928820T>C , CM000685.2:g.154928820T>C GRCh38
NC_000023.10:g.154157095T>C , CM000685.1:g.154157095T>C GRCh37
NC_000023.9:g.153810289T>C NCBI36
NG_011403.1:g.98904A>G
NG_011403.2:g.98904A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4970A>G MANE Select ENSP00000353393.4:p.Gln1657Arg
ENST00000360256.8:c.4970A>G ENSP00000353393.4:p.Gln1657Arg
NM_000132.3:c.4970A>G NP_000123.1:p.Gln1657Arg
XM_011531126.1:c.4865A>G XP_011529428.1:p.Gln1622Arg
NM_000132.4:c.4970A>G MANE Select NP_000123.1:p.Gln1657Arg