Canonical Allele Identifier: CA414915088
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154194369C>G (hg19) chrX:g.154966094C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966094C>G , CM000685.2:g.154966094C>G GRCh38
NC_000023.10:g.154194369C>G , CM000685.1:g.154194369C>G GRCh37
NC_000023.9:g.153847563C>G NCBI36
NG_011403.1:g.61630G>C
NG_011403.2:g.61630G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1319G>C MANE Select ENSP00000353393.4:p.Arg440Thr
ENST00000647125.1:c.*1195G>C ENSP00000496062.1:n.*1195G>C
ENST00000360256.8:c.1319G>C ENSP00000353393.4:p.Arg440Thr
ENST00000483822.2:n.139G>C
NM_000132.3:c.1319G>C NP_000123.1:p.Arg440Thr
XM_011531126.1:c.1214G>C XP_011529428.1:p.Arg405Thr
NM_000132.4:c.1319G>C MANE Select NP_000123.1:p.Arg440Thr
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