Canonical Allele Identifier: CA414913414
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154928569A>T , CM000685.2:g.154928569A>T GRCh38
NC_000023.10:g.154156844A>T , CM000685.1:g.154156844A>T GRCh37
NC_000023.9:g.153810038A>T NCBI36
NG_011403.1:g.99155T>A
NG_011403.2:g.99155T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5219+2T>A MANE Select ENSP00000353393.4:n.5219+2T>A
ENST00000360256.8:c.5219+2T>A ENSP00000353393.4:n.5219+2T>A
NM_000132.3:c.5219+2T>A NP_000123.1:n.5219+2T>A
XM_011531126.1:c.5114+2T>A XP_011529428.1:n.5114+2T>A
NM_000132.4:c.5219+2T>A MANE Select NP_000123.1:n.5219+2T>A