Canonical Allele Identifier: CA337316002
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs782110498
gnomAD v2: X-154124638-G-A
gnomAD v3: X-154896363-G-A
gnomAD v4: X-154896363-G-A
MyVariant Identifiers: chrX:g.154124638G>A (hg19) chrX:g.154896363G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896363G>A , CM000685.2:g.154896363G>A GRCh38
NC_000023.10:g.154124638G>A , CM000685.1:g.154124638G>A GRCh37
NC_000023.9:g.153777832G>A NCBI36
NG_011403.1:g.131361C>T
NG_011403.2:g.131361C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6274-131C>T MANE Select ENSP00000353393.4:n.6274-131C>T
ENST00000360256.8:c.6274-131C>T ENSP00000353393.4:n.6274-131C>T
NM_000132.3:c.6274-131C>T NP_000123.1:n.6274-131C>T
XM_011531126.1:c.6169-131C>T XP_011529428.1:n.6169-131C>T
NM_000132.4:c.6274-131C>T MANE Select NP_000123.1:n.6274-131C>T
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