Canonical Allele Identifier: CA337319306

Gene: F8

Linked Data

• dbSNP Id: rs954942091
• gnomAD v2: X-154065764-T-C
• gnomAD v3: X-154837489-T-C
• gnomAD v4: X-154837489-T-C
• MyVariant Identifiers: chrX:g.154065764T>C (hg19) ; chrX:g.154837489T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837489T>C , CM000685.2:g.154837489T>C	GRCh38
NC_000023.10:g.154065764T>C , CM000685.1:g.154065764T>C	GRCh37
NC_000023.9:g.153718958T>C	NCBI36
NG_011403.1:g.190235A>G
NG_033065.1:g.2174A>G
NG_011403.2:g.190235A>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.*108A>G MANE Select	ENSP00000353393.4:n.*108A>G
ENST00000644698.1:c.*108A>G	ENSP00000495706.1:n.*108A>G
ENST00000330287.10:c.*108A>G	ENSP00000327895.6:n.*108A>G
ENST00000360256.8:c.*108A>G	ENSP00000353393.4:n.*108A>G
NM_000132.3:c.*108A>G	NP_000123.1:n.*108A>G
NM_019863.2:c.*108A>G	NP_063916.1:n.*108A>G
XM_011531126.1:c.*108A>G	XP_011529428.1:n.*108A>G
NM_000132.4:c.*108A>G MANE Select	NP_000123.1:n.*108A>G
NM_019863.3:c.*108A>G	NP_063916.1:n.*108A>G