Canonical Allele Identifier: CA414906106
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154132279C>A (hg19) chrX:g.154904004C>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904004C>A , CM000685.2:g.154904004C>A GRCh38
NC_000023.10:g.154132279C>A , CM000685.1:g.154132279C>A GRCh37
NC_000023.9:g.153785473C>A NCBI36
NG_011403.1:g.123720G>T
NG_011403.2:g.123720G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5900G>T MANE Select ENSP00000353393.4:p.Gly1967Val
ENST00000360256.8:c.5900G>T ENSP00000353393.4:p.Gly1967Val
NM_000132.3:c.5900G>T NP_000123.1:p.Gly1967Val
XM_011531126.1:c.5795G>T XP_011529428.1:p.Gly1932Val
NM_000132.4:c.5900G>T MANE Select NP_000123.1:p.Gly1967Val
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