Canonical Allele Identifier: CA645246762
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1282959661
gnomAD v2: X-154221695-A-T
gnomAD v3: X-154993420-A-T
gnomAD v4: X-154993420-A-T
MyVariant Identifiers: chrX:g.154221695A>T (hg19) chrX:g.154993420A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154993420A>T , CM000685.2:g.154993420A>T GRCh38
NC_000023.10:g.154221695A>T , CM000685.1:g.154221695A>T GRCh37
NC_000023.9:g.153874889A>T NCBI36
NG_011403.1:g.34304T>A
NG_011403.2:g.34304T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.389-272T>A MANE Select ENSP00000353393.4:n.389-272T>A
ENST00000647125.1:c.*175-272T>A ENSP00000496062.1:n.*175-272T>A
ENST00000360256.8:c.389-272T>A ENSP00000353393.4:n.389-272T>A
ENST00000423959.5:c.284-272T>A ENSP00000409446.1:n.284-272T>A
ENST00000453950.1:c.371-272T>A ENSP00000389153.1:n.371-272T>A
NM_000132.3:c.389-272T>A NP_000123.1:n.389-272T>A
XM_011531126.1:c.284-272T>A XP_011529428.1:n.284-272T>A
NM_000132.4:c.389-272T>A MANE Select NP_000123.1:n.389-272T>A
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