Canonical Allele Identifier: CA1138612634
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073766098
gnomAD v3: X-155022648-G-C
gnomAD v4: X-155022648-G-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022648G>C , CM000685.2:g.155022648G>C GRCh38
NC_000023.10:g.154250923G>C , CM000685.1:g.154250923G>C GRCh37
NC_000023.9:g.153904117G>C NCBI36
NG_011403.1:g.5076C>G
NG_011403.2:g.5076C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.-96C>G MANE Select ENSP00000353393.4:n.-96C>G
ENST00000647125.1:c.-96C>G ENSP00000496062.1:n.-96C>G
ENST00000360256.8:c.-96C>G ENSP00000353393.4:n.-96C>G
ENST00000423959.5:c.38+4132C>G ENSP00000409446.1:n.38+4132C>G
ENST00000453950.1:c.39-152C>G ENSP00000389153.1:n.39-152C>G
NM_000132.3:c.-96C>G NP_000123.1:n.-96C>G
XM_011531126.1:c.38+4132C>G XP_011529428.1:n.38+4132C>G
NM_000132.4:c.-96C>G MANE Select NP_000123.1:n.-96C>G
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