Canonical Allele Identifier: CA414913515
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154928595-C-T
MyVariant Identifiers: chrX:g.154156870C>T (hg19) chrX:g.154928595C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928595C>T , CM000685.2:g.154928595C>T GRCh38
NC_000023.10:g.154156870C>T , CM000685.1:g.154156870C>T GRCh37
NC_000023.9:g.153810064C>T NCBI36
NG_011403.1:g.99129G>A
NG_011403.2:g.99129G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5195G>A MANE Select ENSP00000353393.4:p.Ser1732Asn
ENST00000360256.8:c.5195G>A ENSP00000353393.4:p.Ser1732Asn
NM_000132.3:c.5195G>A NP_000123.1:p.Ser1732Asn
XM_011531126.1:c.5090G>A XP_011529428.1:p.Ser1697Asn
NM_000132.4:c.5195G>A MANE Select NP_000123.1:p.Ser1732Asn
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