Canonical Allele Identifier: CA2695237975
Gene: F8 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904048_154904049dup , CM000685.2:g.154904048_154904049dup GRCh38
NC_000023.10:g.154132323_154132324dup , CM000685.1:g.154132323_154132324dup GRCh37
NC_000023.9:g.153785517_153785518dup NCBI36
NG_011403.1:g.123675_123676dup
NG_011403.2:g.123675_123676dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5855_5856dup MANE Select ENSP00000353393.4:p.Met1953Ter
ENST00000360256.8:c.5855_5856dup ENSP00000353393.4:p.Met1953Ter
NM_000132.3:c.5855_5856dup NP_000123.1:p.Met1953Ter
XM_011531126.1:c.5750_5751dup XP_011529428.1:p.Met1918Ter
NM_000132.4:c.5855_5856dup MANE Select NP_000123.1:p.Met1953Ter
Search 100 bp 5'
Search 100 bp 3'