Canonical Allele Identifier: CA414915360
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154157168T>G (hg19) chrX:g.154928893T>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928893T>G , CM000685.2:g.154928893T>G GRCh38
NC_000023.10:g.154157168T>G , CM000685.1:g.154157168T>G GRCh37
NC_000023.9:g.153810362T>G NCBI36
NG_011403.1:g.98831A>C
NG_011403.2:g.98831A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4897A>C MANE Select ENSP00000353393.4:p.Asn1633His
ENST00000360256.8:c.4897A>C ENSP00000353393.4:p.Asn1633His
NM_000132.3:c.4897A>C NP_000123.1:p.Asn1633His
XM_011531126.1:c.4792A>C XP_011529428.1:p.Asn1598His
NM_000132.4:c.4897A>C MANE Select NP_000123.1:p.Asn1633His
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