Canonical Allele Identifier: CA519355294

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154065986G>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837711G>A , CM000685.2:g.154837711G>A	GRCh38
NC_000023.10:g.154065986G>A , CM000685.1:g.154065986G>A	GRCh37
NC_000023.9:g.153719180G>A	NCBI36
NG_011403.1:g.190013C>T
NG_033065.1:g.1952C>T
NG_011403.2:g.190013C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6942C>T MANE Select	ENSP00000353393.4:p.Asn2314=
ENST00000644698.1:c.675C>T	ENSP00000495706.1:p.Asn225=
ENST00000330287.10:c.537C>T	ENSP00000327895.6:p.Asn179=
ENST00000360256.8:c.6942C>T	ENSP00000353393.4:p.Asn2314=
NM_000132.3:c.6942C>T	NP_000123.1:p.Asn2314=
NM_019863.2:c.537C>T	NP_063916.1:p.Asn179=
XM_011531126.1:c.6837C>T	XP_011529428.1:p.Asn2279=
NM_000132.4:c.6942C>T MANE Select	NP_000123.1:p.Asn2314=
NM_019863.3:c.537C>T	NP_063916.1:p.Asn179=