Canonical Allele Identifier: CA414917901
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154197692G>T (hg19) chrX:g.154969417G>T (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969417G>T , CM000685.2:g.154969417G>T GRCh38
NC_000023.10:g.154197692G>T , CM000685.1:g.154197692G>T GRCh37
NC_000023.9:g.153850886G>T NCBI36
NG_011403.1:g.58307C>A
NG_011403.2:g.58307C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.923C>A MANE Select ENSP00000353393.4:p.Ser308Ter
ENST00000647125.1:c.*799C>A ENSP00000496062.1:n.*799C>A
ENST00000360256.8:c.923C>A ENSP00000353393.4:p.Ser308Ter
NM_000132.3:c.923C>A NP_000123.1:p.Ser308Ter
XM_011531126.1:c.818C>A XP_011529428.1:p.Ser273Ter
NM_000132.4:c.923C>A MANE Select NP_000123.1:p.Ser308Ter
Search 100 bp 5'
Search 100 bp 3'