Canonical Allele Identifier: CA2695167701

Gene: F8

Linked Data

• gnomAD v4: X-154860355-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860355T>G , CM000685.2:g.154860355T>G	GRCh38
NC_000023.10:g.154088630T>G , CM000685.1:g.154088630T>G	GRCh37
NC_000023.9:g.153741824T>G	NCBI36
NG_011403.1:g.167369A>C
NG_011403.2:g.167369A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6900+77A>C MANE Select	ENSP00000353393.4:n.6900+77A>C
ENST00000644698.1:c.633+77A>C	ENSP00000495706.1:n.633+77A>C
ENST00000330287.10:c.495+77A>C	ENSP00000327895.6:n.495+77A>C
ENST00000360256.8:c.6900+77A>C	ENSP00000353393.4:n.6900+77A>C
NM_000132.3:c.6900+77A>C	NP_000123.1:n.6900+77A>C
NM_019863.2:c.495+77A>C	NP_063916.1:n.495+77A>C
XM_011531126.1:c.6795+77A>C	XP_011529428.1:n.6795+77A>C
NM_000132.4:c.6900+77A>C MANE Select	NP_000123.1:n.6900+77A>C
NM_019863.3:c.495+77A>C	NP_063916.1:n.495+77A>C