Canonical Allele Identifier: CA414906809
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863087T>G , CM000685.2:g.154863087T>G GRCh38
NC_000023.10:g.154091362T>G , CM000685.1:g.154091362T>G GRCh37
NC_000023.9:g.153744556T>G NCBI36
NG_011403.1:g.164637A>C
NG_011403.2:g.164637A>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6570A>C MANE Select ENSP00000353393.4:p.Leu2190Phe
ENST00000644698.1:c.303A>C ENSP00000495706.1:p.Leu101Phe
ENST00000330287.10:c.165A>C ENSP00000327895.6:p.Leu55Phe
ENST00000360256.8:c.6570A>C ENSP00000353393.4:p.Leu2190Phe
NM_000132.3:c.6570A>C NP_000123.1:p.Leu2190Phe
NM_019863.2:c.165A>C NP_063916.1:p.Leu55Phe
XM_011531126.1:c.6465A>C XP_011529428.1:p.Leu2155Phe
NM_000132.4:c.6570A>C MANE Select NP_000123.1:p.Leu2190Phe
NM_019863.3:c.165A>C NP_063916.1:p.Leu55Phe