Canonical Allele Identifier: CA2466849005
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2073443285
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969430_154969431insAATCT , CM000685.2:g.154969430_154969431insAATCT GRCh38
NC_000023.10:g.154197705_154197706insAATCT , CM000685.1:g.154197705_154197706insAATCT GRCh37
NC_000023.9:g.153850899_153850900insAATCT NCBI36
NG_011403.1:g.58293_58294insAGATT
NG_011403.2:g.58293_58294insAGATT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.909_910insAGATT MANE Select ENSP00000353393.4:p.Ser304ArgfsTer9
ENST00000647125.1:c.*785_*786insAGATT ENSP00000496062.1:n.*785_*786insAGATT
ENST00000360256.8:c.909_910insAGATT ENSP00000353393.4:p.Ser304ArgfsTer9
NM_000132.3:c.909_910insAGATT NP_000123.1:p.Ser304ArgfsTer9
XM_011531126.1:c.804_805insAGATT XP_011529428.1:p.Ser269ArgfsTer9
NM_000132.4:c.909_910insAGATT MANE Select NP_000123.1:p.Ser304ArgfsTer9
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