Canonical Allele Identifier: CA414907147
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863119T>G , CM000685.2:g.154863119T>G GRCh38
NC_000023.10:g.154091394T>G , CM000685.1:g.154091394T>G GRCh37
NC_000023.9:g.153744588T>G NCBI36
NG_011403.1:g.164605A>C
NG_011403.2:g.164605A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6538A>C MANE Select ENSP00000353393.4:p.Thr2180Pro
ENST00000644698.1:c.271A>C ENSP00000495706.1:p.Thr91Pro
ENST00000330287.10:c.133A>C ENSP00000327895.6:p.Thr45Pro
ENST00000360256.8:c.6538A>C ENSP00000353393.4:p.Thr2180Pro
NM_000132.3:c.6538A>C NP_000123.1:p.Thr2180Pro
NM_019863.2:c.133A>C NP_063916.1:p.Thr45Pro
XM_011531126.1:c.6433A>C XP_011529428.1:p.Thr2145Pro
NM_000132.4:c.6538A>C MANE Select NP_000123.1:p.Thr2180Pro
NM_019863.3:c.133A>C NP_063916.1:p.Thr45Pro