Canonical Allele Identifier: CA2695237871

Gene: F8

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154902048C>G , CM000685.2:g.154902048C>G	GRCh38
NC_000023.10:g.154130323C>G , CM000685.1:g.154130323C>G	GRCh37
NC_000023.9:g.153783517C>G	NCBI36
NG_011403.1:g.125676G>C
NG_011403.2:g.125676G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6115+3G>C MANE Select	ENSP00000353393.4:n.6115+3G>C
ENST00000360256.8:c.6115+3G>C	ENSP00000353393.4:n.6115+3G>C
NM_000132.3:c.6115+3G>C	NP_000123.1:n.6115+3G>C
XM_011531126.1:c.6010+3G>C	XP_011529428.1:n.6010+3G>C
NM_000132.4:c.6115+3G>C MANE Select	NP_000123.1:n.6115+3G>C