Canonical Allele Identifier: CA414915507
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154157187A>C (hg19) chrX:g.154928912A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928912A>C , CM000685.2:g.154928912A>C GRCh38
NC_000023.10:g.154157187A>C , CM000685.1:g.154157187A>C GRCh37
NC_000023.9:g.153810381A>C NCBI36
NG_011403.1:g.98812T>G
NG_011403.2:g.98812T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4878T>G MANE Select ENSP00000353393.4:p.Asn1626Lys
ENST00000360256.8:c.4878T>G ENSP00000353393.4:p.Asn1626Lys
NM_000132.3:c.4878T>G NP_000123.1:p.Asn1626Lys
XM_011531126.1:c.4773T>G XP_011529428.1:p.Asn1591Lys
NM_000132.4:c.4878T>G MANE Select NP_000123.1:p.Asn1626Lys
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