Canonical Allele Identifier: CA337326888

Gene: F8

Linked Data

• dbSNP Id: rs945043276
• gnomAD v4: X-154862941-G-T
• MyVariant Identifiers: chrX:g.154862941G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154862941G>T , CM000685.2:g.154862941G>T	GRCh38
NC_000023.10:g.154091216G>T , CM000685.1:g.154091216G>T	GRCh37
NC_000023.9:g.153744410G>T	NCBI36
NG_011403.1:g.164783C>A
NG_011403.2:g.164783C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6574+142C>A MANE Select	ENSP00000353393.4:n.6574+142C>A
ENST00000644698.1:c.307+142C>A	ENSP00000495706.1:n.307+142C>A
ENST00000330287.10:c.169+142C>A	ENSP00000327895.6:n.169+142C>A
ENST00000360256.8:c.6574+142C>A	ENSP00000353393.4:n.6574+142C>A
NM_000132.3:c.6574+142C>A	NP_000123.1:n.6574+142C>A
NM_019863.2:c.169+142C>A	NP_063916.1:n.169+142C>A
XM_011531126.1:c.6469+142C>A	XP_011529428.1:n.6469+142C>A
NM_000132.4:c.6574+142C>A MANE Select	NP_000123.1:n.6574+142C>A
NM_019863.3:c.169+142C>A	NP_063916.1:n.169+142C>A