Canonical Allele Identifier: CA519355322

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154066022A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837747A>G , CM000685.2:g.154837747A>G	GRCh38
NC_000023.10:g.154066022A>G , CM000685.1:g.154066022A>G	GRCh37
NC_000023.9:g.153719216A>G	NCBI36
NG_011403.1:g.189977T>C
NG_033065.1:g.1916T>C
NG_011403.2:g.189977T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6906T>C MANE Select	ENSP00000353393.4:p.Phe2302=
ENST00000644698.1:c.639T>C	ENSP00000495706.1:p.Phe213=
ENST00000330287.10:c.501T>C	ENSP00000327895.6:p.Phe167=
ENST00000360256.8:c.6906T>C	ENSP00000353393.4:p.Phe2302=
NM_000132.3:c.6906T>C	NP_000123.1:p.Phe2302=
NM_019863.2:c.501T>C	NP_063916.1:p.Phe167=
XM_011531126.1:c.6801T>C	XP_011529428.1:p.Phe2267=
NM_000132.4:c.6906T>C MANE Select	NP_000123.1:p.Phe2302=
NM_019863.3:c.501T>C	NP_063916.1:p.Phe167=