Canonical Allele Identifier: CA2466827663
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154902163_154902170delinsAACACCTT , CM000685.2:g.154902163_154902170delinsAACACCTT GRCh38
NC_000023.10:g.154130438_154130445delinsAACACCTT , CM000685.1:g.154130438_154130445delinsAACACCTT GRCh37
NC_000023.9:g.153783632_153783639delinsAACACCTT NCBI36
NG_011403.1:g.125554_125561delinsAAGGTGTT
NG_011403.2:g.125554_125561delinsAAGGTGTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.5999-3_6003delinsAAGGTGTT
ENST00000360256.8:c.5999-3_6003delinsAAGGTGTT
NM_000132.3:c.5999-3_6003delinsAAGGTGTT
XM_011531126.1:c.5894-3_5898delinsAAGGTGTT
NM_000132.4:c.5999-3_6003delinsAAGGTGTT