Canonical Allele Identifier: CA414911933
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154185362G>C (hg19) chrX:g.154957087G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154957087G>C , CM000685.2:g.154957087G>C GRCh38
NC_000023.10:g.154185362G>C , CM000685.1:g.154185362G>C GRCh37
NC_000023.9:g.153838556G>C NCBI36
NG_011403.1:g.70637C>G
NG_011403.2:g.70637C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1622C>G MANE Select ENSP00000353393.4:p.Thr541Ser
ENST00000647125.1:c.*1498C>G ENSP00000496062.1:n.*1498C>G
ENST00000360256.8:c.1622C>G ENSP00000353393.4:p.Thr541Ser
NM_000132.3:c.1622C>G NP_000123.1:p.Thr541Ser
XM_011531126.1:c.1517C>G XP_011529428.1:p.Thr506Ser
NM_000132.4:c.1622C>G MANE Select NP_000123.1:p.Thr541Ser
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