Canonical Allele Identifier: CA519718452
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1213666821
MyVariant Identifiers: chrX:g.154157081A>G (hg19) chrX:g.154928806A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928806A>G , CM000685.2:g.154928806A>G GRCh38
NC_000023.10:g.154157081A>G , CM000685.1:g.154157081A>G GRCh37
NC_000023.9:g.153810275A>G NCBI36
NG_011403.1:g.98918T>C
NG_011403.2:g.98918T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.4984T>C MANE Select ENSP00000353393.4:p.Leu1662=
ENST00000360256.8:c.4984T>C ENSP00000353393.4:p.Leu1662=
NM_000132.3:c.4984T>C NP_000123.1:p.Leu1662=
XM_011531126.1:c.4879T>C XP_011529428.1:p.Leu1627=
NM_000132.4:c.4984T>C MANE Select NP_000123.1:p.Leu1662=
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