Canonical Allele Identifier: CA414913535
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928599T>C , CM000685.2:g.154928599T>C GRCh38
NC_000023.10:g.154156874T>C , CM000685.1:g.154156874T>C GRCh37
NC_000023.9:g.153810068T>C NCBI36
NG_011403.1:g.99125A>G
NG_011403.2:g.99125A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5191A>G MANE Select ENSP00000353393.4:p.Ser1731Gly
ENST00000360256.8:c.5191A>G ENSP00000353393.4:p.Ser1731Gly
NM_000132.3:c.5191A>G NP_000123.1:p.Ser1731Gly
XM_011531126.1:c.5086A>G XP_011529428.1:p.Ser1696Gly
NM_000132.4:c.5191A>G MANE Select NP_000123.1:p.Ser1731Gly