Canonical Allele Identifier: CA2466815585
Gene: F8 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863103A= , CM000685.2:g.154863103A= GRCh38
NC_000023.10:g.154091378A= , CM000685.1:g.154091378A= GRCh37
NC_000023.9:g.153744572A= NCBI36
NG_011403.1:g.164621T=
NG_011403.2:g.164621T=

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6554T= MANE Select ENSP00000353393.4:p.Leu2185=
ENST00000644698.1:c.287T= ENSP00000495706.1:p.Leu96=
ENST00000330287.10:c.149T= ENSP00000327895.6:p.Leu50=
ENST00000360256.8:c.6554T= ENSP00000353393.4:p.Leu2185=
NM_000132.3:c.6554T= NP_000123.1:p.Leu2185=
NM_019863.2:c.149T= NP_063916.1:p.Leu50=
XM_011531126.1:c.6449T= XP_011529428.1:p.Leu2150=
NM_000132.4:c.6554T= MANE Select NP_000123.1:p.Leu2185=
NM_019863.3:c.149T= NP_063916.1:p.Leu50=