Canonical Allele Identifier: CA519718453
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154157082G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928807G>A , CM000685.2:g.154928807G>A GRCh38
NC_000023.10:g.154157082G>A , CM000685.1:g.154157082G>A GRCh37
NC_000023.9:g.153810276G>A NCBI36
NG_011403.1:g.98917C>T
NG_011403.2:g.98917C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4983C>T MANE Select ENSP00000353393.4:p.Val1661=
ENST00000360256.8:c.4983C>T ENSP00000353393.4:p.Val1661=
NM_000132.3:c.4983C>T NP_000123.1:p.Val1661=
XM_011531126.1:c.4878C>T XP_011529428.1:p.Val1626=
NM_000132.4:c.4983C>T MANE Select NP_000123.1:p.Val1661=
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