Canonical Allele Identifier: CA414907900
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863205G>C , CM000685.2:g.154863205G>C GRCh38
NC_000023.10:g.154091480G>C , CM000685.1:g.154091480G>C GRCh37
NC_000023.9:g.153744674G>C NCBI36
NG_011403.1:g.164519C>G
NG_011403.2:g.164519C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6452C>G MANE Select ENSP00000353393.4:p.Ser2151Ter
ENST00000644698.1:c.185C>G ENSP00000495706.1:p.Ser62Ter
ENST00000330287.10:c.47C>G ENSP00000327895.6:p.Ser16Ter
ENST00000360256.8:c.6452C>G ENSP00000353393.4:p.Ser2151Ter
NM_000132.3:c.6452C>G NP_000123.1:p.Ser2151Ter
NM_019863.2:c.47C>G NP_063916.1:p.Ser16Ter
XM_011531126.1:c.6347C>G XP_011529428.1:p.Ser2116Ter
NM_000132.4:c.6452C>G MANE Select NP_000123.1:p.Ser2151Ter
NM_019863.3:c.47C>G NP_063916.1:p.Ser16Ter