Canonical Allele Identifier: CA2695168132

Gene: F8

Linked Data

• gnomAD v4: X-154904752-T-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904752T>C , CM000685.2:g.154904752T>C	GRCh38
NC_000023.10:g.154133027T>C , CM000685.1:g.154133027T>C	GRCh37
NC_000023.9:g.153786221T>C	NCBI36
NG_011403.1:g.122972A>G
NG_011403.2:g.122972A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5586+59A>G MANE Select	ENSP00000353393.4:n.5586+59A>G
ENST00000360256.8:c.5586+59A>G	ENSP00000353393.4:n.5586+59A>G
NM_000132.3:c.5586+59A>G	NP_000123.1:n.5586+59A>G
XM_011531126.1:c.5481+59A>G	XP_011529428.1:n.5481+59A>G
NM_000132.4:c.5586+59A>G MANE Select	NP_000123.1:n.5586+59A>G