Canonical Allele Identifier: CA519355299

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154065989C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837714C>G , CM000685.2:g.154837714C>G	GRCh38
NC_000023.10:g.154065989C>G , CM000685.1:g.154065989C>G	GRCh37
NC_000023.9:g.153719183C>G	NCBI36
NG_011403.1:g.190010G>C
NG_033065.1:g.1949G>C
NG_011403.2:g.190010G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6939G>C MANE Select	ENSP00000353393.4:p.Val2313=
ENST00000644698.1:c.672G>C	ENSP00000495706.1:p.Val224=
ENST00000330287.10:c.534G>C	ENSP00000327895.6:p.Val178=
ENST00000360256.8:c.6939G>C	ENSP00000353393.4:p.Val2313=
NM_000132.3:c.6939G>C	NP_000123.1:p.Val2313=
NM_019863.2:c.534G>C	NP_063916.1:p.Val178=
XM_011531126.1:c.6834G>C	XP_011529428.1:p.Val2278=
NM_000132.4:c.6939G>C MANE Select	NP_000123.1:p.Val2313=
NM_019863.3:c.534G>C	NP_063916.1:p.Val178=