Canonical Allele Identifier: CA414911950
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154185366G>T (hg19) chrX:g.154957091G>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154957091G>T , CM000685.2:g.154957091G>T GRCh38
NC_000023.10:g.154185366G>T , CM000685.1:g.154185366G>T GRCh37
NC_000023.9:g.153838560G>T NCBI36
NG_011403.1:g.70633C>A
NG_011403.2:g.70633C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1618C>A MANE Select ENSP00000353393.4:p.Pro540Thr
ENST00000647125.1:c.*1494C>A ENSP00000496062.1:n.*1494C>A
ENST00000360256.8:c.1618C>A ENSP00000353393.4:p.Pro540Thr
NM_000132.3:c.1618C>A NP_000123.1:p.Pro540Thr
XM_011531126.1:c.1513C>A XP_011529428.1:p.Pro505Thr
NM_000132.4:c.1618C>A MANE Select NP_000123.1:p.Pro540Thr
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