Canonical Allele Identifier: CA2824302213
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928542G>A , CM000685.2:g.154928542G>A GRCh38
NC_000023.10:g.154156817G>A , CM000685.1:g.154156817G>A GRCh37
NC_000023.9:g.153810011G>A NCBI36
NG_011403.1:g.99182C>T
NG_011403.2:g.99182C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5219+29C>T MANE Select ENSP00000353393.4:n.5219+29C>T
ENST00000360256.8:c.5219+29C>T ENSP00000353393.4:n.5219+29C>T
NM_000132.3:c.5219+29C>T NP_000123.1:n.5219+29C>T
XM_011531126.1:c.5114+29C>T XP_011529428.1:n.5114+29C>T
NM_000132.4:c.5219+29C>T MANE Select NP_000123.1:n.5219+29C>T
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