Canonical Allele Identifier: CA2695169482
Gene: F8 HGNC NCBI

Linked Data

gnomAD v4: X-154965929-T-C
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154965929T>C , CM000685.2:g.154965929T>C GRCh38
NC_000023.10:g.154194204T>C , CM000685.1:g.154194204T>C GRCh37
NC_000023.9:g.153847398T>C NCBI36
NG_011403.1:g.61795A>G
NG_011403.2:g.61795A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1443+41A>G MANE Select ENSP00000353393.4:n.1443+41A>G
ENST00000647125.1:c.*1319+41A>G ENSP00000496062.1:n.*1319+41A>G
ENST00000360256.8:c.1443+41A>G ENSP00000353393.4:n.1443+41A>G
ENST00000483822.2:n.304A>G
NM_000132.3:c.1443+41A>G NP_000123.1:n.1443+41A>G
XM_011531126.1:c.1338+41A>G XP_011529428.1:n.1338+41A>G
NM_000132.4:c.1443+41A>G MANE Select NP_000123.1:n.1443+41A>G
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