Canonical Allele Identifier: CA414913531
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928598C>T , CM000685.2:g.154928598C>T GRCh38
NC_000023.10:g.154156873C>T , CM000685.1:g.154156873C>T GRCh37
NC_000023.9:g.153810067C>T NCBI36
NG_011403.1:g.99126G>A
NG_011403.2:g.99126G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5192G>A MANE Select ENSP00000353393.4:p.Ser1731Asn
ENST00000360256.8:c.5192G>A ENSP00000353393.4:p.Ser1731Asn
NM_000132.3:c.5192G>A NP_000123.1:p.Ser1731Asn
XM_011531126.1:c.5087G>A XP_011529428.1:p.Ser1696Asn
NM_000132.4:c.5192G>A MANE Select NP_000123.1:p.Ser1731Asn