Canonical Allele Identifier: CA873367558
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1317271565
gnomAD v3: X-155022664-C-T
gnomAD v4: X-155022664-C-T
MyVariant Identifiers: chrX:g.155022664C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.155022664C>T , CM000685.2:g.155022664C>T GRCh38
NC_000023.10:g.154250939C>T , CM000685.1:g.154250939C>T GRCh37
NC_000023.9:g.153904133C>T NCBI36
NG_011403.1:g.5060G>A
NG_011403.2:g.5060G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.-112G>A MANE Select ENSP00000353393.4:n.-112G>A
ENST00000647125.1:c.-112G>A ENSP00000496062.1:n.-112G>A
ENST00000360256.8:c.-112G>A ENSP00000353393.4:n.-112G>A
ENST00000423959.5:c.38+4116G>A ENSP00000409446.1:n.38+4116G>A
ENST00000453950.1:c.39-168G>A ENSP00000389153.1:n.39-168G>A
NM_000132.3:c.-112G>A NP_000123.1:n.-112G>A
XM_011531126.1:c.38+4116G>A XP_011529428.1:n.38+4116G>A
NM_000132.4:c.-112G>A MANE Select NP_000123.1:n.-112G>A
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