Canonical Allele Identifier: CA2695152056
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896262_154896265del , CM000685.2:g.154896262_154896265del GRCh38
NC_000023.10:g.154124537_154124540del , CM000685.1:g.154124537_154124540del GRCh37
NC_000023.9:g.153777731_153777734del NCBI36
NG_011403.1:g.131460_131463del
NG_011403.2:g.131460_131463del

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6274-32_6274-29del MANE Select ENSP00000353393.4:n.6274-32_6274-29del
ENST00000360256.8:c.6274-32_6274-29del ENSP00000353393.4:n.6274-32_6274-29del
NM_000132.3:c.6274-32_6274-29del NP_000123.1:n.6274-32_6274-29del
XM_011531126.1:c.6169-32_6169-29del XP_011529428.1:n.6169-32_6169-29del
NM_000132.4:c.6274-32_6274-29del MANE Select NP_000123.1:n.6274-32_6274-29del