Canonical Allele Identifier: CA337319527

Gene: F8

Linked Data

• dbSNP Id: rs996309643
• gnomAD v3: X-154837941-T-G
• gnomAD v4: X-154837941-T-G
• MyVariant Identifiers: chrX:g.154837941T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837941T>G , CM000685.2:g.154837941T>G	GRCh38
NC_000023.10:g.154066216T>G , CM000685.1:g.154066216T>G	GRCh37
NC_000023.9:g.153719410T>G	NCBI36
NG_011403.1:g.189783A>C
NG_033065.1:g.1722A>C
NG_011403.2:g.189783A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6901-189A>C MANE Select	ENSP00000353393.4:n.6901-189A>C
ENST00000644698.1:c.634-189A>C	ENSP00000495706.1:n.634-189A>C
ENST00000330287.10:c.496-189A>C	ENSP00000327895.6:n.496-189A>C
ENST00000360256.8:c.6901-189A>C	ENSP00000353393.4:n.6901-189A>C
NM_000132.3:c.6901-189A>C	NP_000123.1:n.6901-189A>C
NM_019863.2:c.496-189A>C	NP_063916.1:n.496-189A>C
XM_011531126.1:c.6796-189A>C	XP_011529428.1:n.6796-189A>C
NM_000132.4:c.6901-189A>C MANE Select	NP_000123.1:n.6901-189A>C
NM_019863.3:c.496-189A>C	NP_063916.1:n.496-189A>C