Canonical Allele Identifier: CA873360707
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs1313530423

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837514dup , CM000685.2:g.154837514dup GRCh38
NC_000023.10:g.154065789dup , CM000685.1:g.154065789dup GRCh37
NC_000023.9:g.153718983dup NCBI36
NG_011403.1:g.190210dup
NG_033065.1:g.2149dup
NG_011403.2:g.190210dup

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.*83dup MANE Select ENSP00000353393.4:n.*83dup
ENST00000644698.1:c.*83dup ENSP00000495706.1:n.*83dup
ENST00000330287.10:c.*83dup ENSP00000327895.6:n.*83dup
ENST00000360256.8:c.*83dup ENSP00000353393.4:n.*83dup
NM_000132.3:c.*83dup NP_000123.1:n.*83dup
NM_019863.2:c.*83dup NP_063916.1:n.*83dup
XM_011531126.1:c.*83dup XP_011529428.1:n.*83dup
NM_000132.4:c.*83dup MANE Select NP_000123.1:n.*83dup
NM_019863.3:c.*83dup NP_063916.1:n.*83dup