Canonical Allele Identifier: CA2466807340
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs2072482092

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837437del , CM000685.2:g.154837437del GRCh38
NC_000023.10:g.154065712del , CM000685.1:g.154065712del GRCh37
NC_000023.9:g.153718906del NCBI36
NG_011403.1:g.190292del
NG_033065.1:g.2231del
NG_011403.2:g.190292del

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.*165del MANE Select ENSP00000353393.4:n.*165del
ENST00000644698.1:c.*165del ENSP00000495706.1:n.*165del
ENST00000330287.10:c.*165del ENSP00000327895.6:n.*165del
ENST00000360256.8:c.*165del ENSP00000353393.4:n.*165del
NM_000132.3:c.*165del NP_000123.1:n.*165del
NM_019863.2:c.*165del NP_063916.1:n.*165del
XM_011531126.1:c.*165del XP_011529428.1:n.*165del
NM_000132.4:c.*165del MANE Select NP_000123.1:n.*165del
NM_019863.3:c.*165del NP_063916.1:n.*165del