Canonical Allele Identifier: CA645292715
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1299987981
gnomAD v2: X-154132441-A-T
gnomAD v3: X-154904166-A-T
gnomAD v4: X-154904166-A-T
MyVariant Identifiers: chrX:g.154132441A>T (hg19) chrX:g.154904166A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904166A>T , CM000685.2:g.154904166A>T GRCh38
NC_000023.10:g.154132441A>T , CM000685.1:g.154132441A>T GRCh37
NC_000023.9:g.153785635A>T NCBI36
NG_011403.1:g.123558T>A
NG_011403.2:g.123558T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5816-78T>A MANE Select ENSP00000353393.4:n.5816-78T>A
ENST00000360256.8:c.5816-78T>A ENSP00000353393.4:n.5816-78T>A
NM_000132.3:c.5816-78T>A NP_000123.1:n.5816-78T>A
XM_011531126.1:c.5711-78T>A XP_011529428.1:n.5711-78T>A
NM_000132.4:c.5816-78T>A MANE Select NP_000123.1:n.5816-78T>A
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