Canonical Allele Identifier: CA1138596764
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073025022
gnomAD v3: X-154904188-C-T
gnomAD v4: X-154904188-C-T
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904188C>T , CM000685.2:g.154904188C>T GRCh38
NC_000023.10:g.154132463C>T , CM000685.1:g.154132463C>T GRCh37
NC_000023.9:g.153785657C>T NCBI36
NG_011403.1:g.123536G>A
NG_011403.2:g.123536G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5816-100G>A MANE Select ENSP00000353393.4:n.5816-100G>A
ENST00000360256.8:c.5816-100G>A ENSP00000353393.4:n.5816-100G>A
NM_000132.3:c.5816-100G>A NP_000123.1:n.5816-100G>A
XM_011531126.1:c.5711-100G>A XP_011529428.1:n.5711-100G>A
NM_000132.4:c.5816-100G>A MANE Select NP_000123.1:n.5816-100G>A
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