Canonical Allele Identifier: CA414896950
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837655A>C , CM000685.2:g.154837655A>C GRCh38
NC_000023.10:g.154065930A>C , CM000685.1:g.154065930A>C GRCh37
NC_000023.9:g.153719124A>C NCBI36
NG_011403.1:g.190069T>G
NG_033065.1:g.2008T>G
NG_011403.2:g.190069T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6998T>G MANE Select ENSP00000353393.4:p.Val2333Gly
ENST00000644698.1:c.731T>G ENSP00000495706.1:p.Val244Gly
ENST00000330287.10:c.593T>G ENSP00000327895.6:p.Val198Gly
ENST00000360256.8:c.6998T>G ENSP00000353393.4:p.Val2333Gly
NM_000132.3:c.6998T>G NP_000123.1:p.Val2333Gly
NM_019863.2:c.593T>G NP_063916.1:p.Val198Gly
XM_011531126.1:c.6893T>G XP_011529428.1:p.Val2298Gly
NM_000132.4:c.6998T>G MANE Select NP_000123.1:p.Val2333Gly
NM_019863.3:c.593T>G NP_063916.1:p.Val198Gly