Canonical Allele Identifier: CA519717772
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154132290C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904015C>T , CM000685.2:g.154904015C>T GRCh38
NC_000023.10:g.154132290C>T , CM000685.1:g.154132290C>T GRCh37
NC_000023.9:g.153785484C>T NCBI36
NG_011403.1:g.123709G>A
NG_011403.2:g.123709G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5889G>A MANE Select ENSP00000353393.4:p.Leu1963=
ENST00000360256.8:c.5889G>A ENSP00000353393.4:p.Leu1963=
NM_000132.3:c.5889G>A NP_000123.1:p.Leu1963=
XM_011531126.1:c.5784G>A XP_011529428.1:p.Leu1928=
NM_000132.4:c.5889G>A MANE Select NP_000123.1:p.Leu1963=
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