Canonical Allele Identifier: CA10568055
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs200274569
ExAC: X:154157087 G / T
gnomAD v2: X-154157087-G-T
gnomAD v3: X-154928812-G-T
gnomAD v4: X-154928812-G-T
MyVariant Identifiers: chrX:g.154157087G>T (hg19) chrX:g.154928812G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928812G>T , CM000685.2:g.154928812G>T GRCh38
NC_000023.10:g.154157087G>T , CM000685.1:g.154157087G>T GRCh37
NC_000023.9:g.153810281G>T NCBI36
NG_011403.1:g.98912C>A
NG_011403.2:g.98912C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4978C>A MANE Select ENSP00000353393.4:p.Pro1660Thr
ENST00000360256.8:c.4978C>A ENSP00000353393.4:p.Pro1660Thr
NM_000132.3:c.4978C>A NP_000123.1:p.Pro1660Thr
XM_011531126.1:c.4873C>A XP_011529428.1:p.Pro1625Thr
NM_000132.4:c.4978C>A MANE Select NP_000123.1:p.Pro1660Thr
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