Canonical Allele Identifier: CA2695170148
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154993211-A-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154993211A>C , CM000685.2:g.154993211A>C GRCh38
NC_000023.10:g.154221486A>C , CM000685.1:g.154221486A>C GRCh37
NC_000023.9:g.153874680A>C NCBI36
NG_011403.1:g.34513T>G
NG_011403.2:g.34513T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.389-63T>G MANE Select ENSP00000353393.4:n.389-63T>G
ENST00000647125.1:c.*175-63T>G ENSP00000496062.1:n.*175-63T>G
ENST00000360256.8:c.389-63T>G ENSP00000353393.4:n.389-63T>G
ENST00000423959.5:c.284-63T>G ENSP00000409446.1:n.284-63T>G
ENST00000453950.1:c.371-63T>G ENSP00000389153.1:n.371-63T>G
NM_000132.3:c.389-63T>G NP_000123.1:n.389-63T>G
XM_011531126.1:c.284-63T>G XP_011529428.1:n.284-63T>G
NM_000132.4:c.389-63T>G MANE Select NP_000123.1:n.389-63T>G
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