Canonical Allele Identifier: CA519384134
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154225315A>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997040A>C , CM000685.2:g.154997040A>C GRCh38
NC_000023.10:g.154225315A>C , CM000685.1:g.154225315A>C GRCh37
NC_000023.9:g.153878509A>C NCBI36
NG_011403.1:g.30684T>G
NG_011403.2:g.30684T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.321T>G MANE Select ENSP00000353393.4:p.Leu107=
ENST00000647125.1:c.*107T>G ENSP00000496062.1:n.*107T>G
ENST00000360256.8:c.321T>G ENSP00000353393.4:p.Leu107=
ENST00000423959.5:c.216T>G ENSP00000409446.1:p.Leu72=
ENST00000453950.1:c.303T>G ENSP00000389153.1:p.Leu101=
NM_000132.3:c.321T>G NP_000123.1:p.Leu107=
XM_011531126.1:c.216T>G XP_011529428.1:p.Leu72=
NM_000132.4:c.321T>G MANE Select NP_000123.1:p.Leu107=