Canonical Allele Identifier: CA2695170439
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-155022302-C-A
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022302C>A , CM000685.2:g.155022302C>A GRCh38
NC_000023.10:g.154250577C>A , CM000685.1:g.154250577C>A GRCh37
NC_000023.9:g.153903771C>A NCBI36
NG_011403.1:g.5422G>T
NG_011403.2:g.5422G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.143+108G>T MANE Select ENSP00000353393.4:n.143+108G>T
ENST00000647125.1:c.121+130G>T ENSP00000496062.1:n.121+130G>T
ENST00000360256.8:c.143+108G>T ENSP00000353393.4:n.143+108G>T
ENST00000423959.5:c.38+4478G>T ENSP00000409446.1:n.38+4478G>T
ENST00000453950.1:c.125+108G>T ENSP00000389153.1:n.125+108G>T
NM_000132.3:c.143+108G>T NP_000123.1:n.143+108G>T
XM_011531126.1:c.38+4478G>T XP_011529428.1:n.38+4478G>T
NM_000132.4:c.143+108G>T MANE Select NP_000123.1:n.143+108G>T
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