Canonical Allele Identifier: CA645292711
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1205949233
gnomAD v2: X-154132374-A-T
gnomAD v3: X-154904099-A-T
gnomAD v4: X-154904099-A-T
MyVariant Identifiers: chrX:g.154132374A>T (hg19) chrX:g.154904099A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904099A>T , CM000685.2:g.154904099A>T GRCh38
NC_000023.10:g.154132374A>T , CM000685.1:g.154132374A>T GRCh37
NC_000023.9:g.153785568A>T NCBI36
NG_011403.1:g.123625T>A
NG_011403.2:g.123625T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5816-11T>A MANE Select ENSP00000353393.4:n.5816-11T>A
ENST00000360256.8:c.5816-11T>A ENSP00000353393.4:n.5816-11T>A
NM_000132.3:c.5816-11T>A NP_000123.1:n.5816-11T>A
XM_011531126.1:c.5711-11T>A XP_011529428.1:n.5711-11T>A
NM_000132.4:c.5816-11T>A MANE Select NP_000123.1:n.5816-11T>A
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