Canonical Allele Identifier: CA414916722
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966577T>A , CM000685.2:g.154966577T>A GRCh38
NC_000023.10:g.154194852T>A , CM000685.1:g.154194852T>A GRCh37
NC_000023.9:g.153848046T>A NCBI36
NG_011403.1:g.61147A>T
NG_011403.2:g.61147A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1120A>T MANE Select ENSP00000353393.4:p.Met374Leu
ENST00000647125.1:c.*996A>T ENSP00000496062.1:n.*996A>T
ENST00000360256.8:c.1120A>T ENSP00000353393.4:p.Met374Leu
NM_000132.3:c.1120A>T NP_000123.1:p.Met374Leu
XM_011531126.1:c.1015A>T XP_011529428.1:p.Met339Leu
NM_000132.4:c.1120A>T MANE Select NP_000123.1:p.Met374Leu