Canonical Allele Identifier: CA519355170

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154065887T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837612T>G , CM000685.2:g.154837612T>G	GRCh38
NC_000023.10:g.154065887T>G , CM000685.1:g.154065887T>G	GRCh37
NC_000023.9:g.153719081T>G	NCBI36
NG_011403.1:g.190112A>C
NG_033065.1:g.2051A>C
NG_011403.2:g.190112A>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.7041A>C MANE Select	ENSP00000353393.4:p.Ala2347=
ENST00000644698.1:c.774A>C	ENSP00000495706.1:p.Ala258=
ENST00000330287.10:c.636A>C	ENSP00000327895.6:p.Ala212=
ENST00000360256.8:c.7041A>C	ENSP00000353393.4:p.Ala2347=
NM_000132.3:c.7041A>C	NP_000123.1:p.Ala2347=
NM_019863.2:c.636A>C	NP_063916.1:p.Ala212=
XM_011531126.1:c.6936A>C	XP_011529428.1:p.Ala2312=
NM_000132.4:c.7041A>C MANE Select	NP_000123.1:p.Ala2347=
NM_019863.3:c.636A>C	NP_063916.1:p.Ala212=