Canonical Allele Identifier: CA414906495
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154132328A>C (hg19) chrX:g.154904053A>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904053A>C , CM000685.2:g.154904053A>C GRCh38
NC_000023.10:g.154132328A>C , CM000685.1:g.154132328A>C GRCh37
NC_000023.9:g.153785522A>C NCBI36
NG_011403.1:g.123671T>G
NG_011403.2:g.123671T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5851T>G MANE Select ENSP00000353393.4:p.Leu1951Val
ENST00000360256.8:c.5851T>G ENSP00000353393.4:p.Leu1951Val
NM_000132.3:c.5851T>G NP_000123.1:p.Leu1951Val
XM_011531126.1:c.5746T>G XP_011529428.1:p.Leu1916Val
NM_000132.4:c.5851T>G MANE Select NP_000123.1:p.Leu1951Val
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