Canonical Allele Identifier: CA519388692
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154250752G>A (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022477G>A , CM000685.2:g.155022477G>A GRCh38
NC_000023.10:g.154250752G>A , CM000685.1:g.154250752G>A GRCh37
NC_000023.9:g.153903946G>A NCBI36
NG_011403.1:g.5247C>T
NG_011403.2:g.5247C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.76C>T MANE Select ENSP00000353393.4:p.Leu26=
ENST00000647125.1:c.76C>T ENSP00000496062.1:p.Leu26=
ENST00000360256.8:c.76C>T ENSP00000353393.4:p.Leu26=
ENST00000423959.5:c.38+4303C>T ENSP00000409446.1:n.38+4303C>T
ENST00000453950.1:c.58C>T ENSP00000389153.1:p.Leu20=
NM_000132.3:c.76C>T NP_000123.1:p.Leu26=
XM_011531126.1:c.38+4303C>T XP_011529428.1:n.38+4303C>T
NM_000132.4:c.76C>T MANE Select NP_000123.1:p.Leu26=
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