Canonical Allele Identifier: CA414906212
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154132292G>T (hg19) chrX:g.154904017G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904017G>T , CM000685.2:g.154904017G>T GRCh38
NC_000023.10:g.154132292G>T , CM000685.1:g.154132292G>T GRCh37
NC_000023.9:g.153785486G>T NCBI36
NG_011403.1:g.123707C>A
NG_011403.2:g.123707C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5887C>A MANE Select ENSP00000353393.4:p.Leu1963Met
ENST00000360256.8:c.5887C>A ENSP00000353393.4:p.Leu1963Met
NM_000132.3:c.5887C>A NP_000123.1:p.Leu1963Met
XM_011531126.1:c.5782C>A XP_011529428.1:p.Leu1928Met
NM_000132.4:c.5887C>A MANE Select NP_000123.1:p.Leu1963Met
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