Canonical Allele Identifier: CA414913422

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154156845C>G (hg19) ; chrX:g.154928570C>G (hg38)

Genomic Alleles

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

Transcript Alleles

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