Canonical Allele Identifier: CA414913418
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928570C>A , CM000685.2:g.154928570C>A GRCh38
NC_000023.10:g.154156845C>A , CM000685.1:g.154156845C>A GRCh37
NC_000023.9:g.153810039C>A NCBI36
NG_011403.1:g.99154G>T
NG_011403.2:g.99154G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5219+1G>T MANE Select ENSP00000353393.4:n.5219+1G>T
ENST00000360256.8:c.5219+1G>T ENSP00000353393.4:n.5219+1G>T
NM_000132.3:c.5219+1G>T NP_000123.1:n.5219+1G>T
XM_011531126.1:c.5114+1G>T XP_011529428.1:n.5114+1G>T
NM_000132.4:c.5219+1G>T MANE Select NP_000123.1:n.5219+1G>T