Canonical Allele Identifier: CA414911340
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154182318C>T (hg19) chrX:g.154954043C>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154954043C>T , CM000685.2:g.154954043C>T GRCh38
NC_000023.10:g.154182318C>T , CM000685.1:g.154182318C>T GRCh37
NC_000023.9:g.153835512C>T NCBI36
NG_011403.1:g.73681G>A
NG_011403.2:g.73681G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1753-1G>A MANE Select ENSP00000353393.4:n.1753-1G>A
ENST00000647125.1:c.*1629-1G>A ENSP00000496062.1:n.*1629-1G>A
ENST00000360256.8:c.1753-1G>A ENSP00000353393.4:n.1753-1G>A
NM_000132.3:c.1753-1G>A NP_000123.1:n.1753-1G>A
XM_011531126.1:c.1648-1G>A XP_011529428.1:n.1648-1G>A
NM_000132.4:c.1753-1G>A MANE Select NP_000123.1:n.1753-1G>A
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