Canonical Allele Identifier: CA414901696
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154159627A>G (hg19) chrX:g.154931352A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154931352A>G , CM000685.2:g.154931352A>G GRCh38
NC_000023.10:g.154159627A>G , CM000685.1:g.154159627A>G GRCh37
NC_000023.9:g.153812821A>G NCBI36
NG_011403.1:g.96372T>C
NG_011403.2:g.96372T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.2438T>C MANE Select ENSP00000353393.4:p.Leu813Ser
ENST00000647125.1:c.*2104T>C ENSP00000496062.1:n.*2104T>C
ENST00000360256.8:c.2438T>C ENSP00000353393.4:p.Leu813Ser
NM_000132.3:c.2438T>C NP_000123.1:p.Leu813Ser
XM_011531126.1:c.2333T>C XP_011529428.1:p.Leu778Ser
NM_000132.4:c.2438T>C MANE Select NP_000123.1:p.Leu813Ser
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