Canonical Allele Identifier: CA414897568
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837719C>T , CM000685.2:g.154837719C>T GRCh38
NC_000023.10:g.154065994C>T , CM000685.1:g.154065994C>T GRCh37
NC_000023.9:g.153719188C>T NCBI36
NG_011403.1:g.190005G>A
NG_033065.1:g.1944G>A
NG_011403.2:g.190005G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6934G>A MANE Select ENSP00000353393.4:p.Val2312Met
ENST00000644698.1:c.667G>A ENSP00000495706.1:p.Val223Met
ENST00000330287.10:c.529G>A ENSP00000327895.6:p.Val177Met
ENST00000360256.8:c.6934G>A ENSP00000353393.4:p.Val2312Met
NM_000132.3:c.6934G>A NP_000123.1:p.Val2312Met
NM_019863.2:c.529G>A NP_063916.1:p.Val177Met
XM_011531126.1:c.6829G>A XP_011529428.1:p.Val2277Met
NM_000132.4:c.6934G>A MANE Select NP_000123.1:p.Val2312Met
NM_019863.3:c.529G>A NP_063916.1:p.Val177Met