Canonical Allele Identifier: CA414906355
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154904038-C-G
MyVariant Identifiers: chrX:g.154132313C>G (hg19) chrX:g.154904038C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904038C>G , CM000685.2:g.154904038C>G GRCh38
NC_000023.10:g.154132313C>G , CM000685.1:g.154132313C>G GRCh37
NC_000023.9:g.153785507C>G NCBI36
NG_011403.1:g.123686G>C
NG_011403.2:g.123686G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5866G>C MANE Select ENSP00000353393.4:p.Asp1956His
ENST00000360256.8:c.5866G>C ENSP00000353393.4:p.Asp1956His
NM_000132.3:c.5866G>C NP_000123.1:p.Asp1956His
XM_011531126.1:c.5761G>C XP_011529428.1:p.Asp1921His
NM_000132.4:c.5866G>C MANE Select NP_000123.1:p.Asp1956His
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