Canonical Allele Identifier: CA414904435

Gene: F8

Linked Data

• dbSNP Id: rs1216018493
• MyVariant Identifiers: chrX:g.154088835T>A (hg19) ; chrX:g.154860560T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860560T>A , CM000685.2:g.154860560T>A	GRCh38
NC_000023.10:g.154088835T>A , CM000685.1:g.154088835T>A	GRCh37
NC_000023.9:g.153742029T>A	NCBI36
NG_011403.1:g.167164A>T
NG_011403.2:g.167164A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6772A>T MANE Select	ENSP00000353393.4:p.Lys2258Ter
ENST00000644698.1:c.505A>T	ENSP00000495706.1:p.Lys169Ter
ENST00000330287.10:c.367A>T	ENSP00000327895.6:p.Lys123Ter
ENST00000360256.8:c.6772A>T	ENSP00000353393.4:p.Lys2258Ter
NM_000132.3:c.6772A>T	NP_000123.1:p.Lys2258Ter
NM_019863.2:c.367A>T	NP_063916.1:p.Lys123Ter
XM_011531126.1:c.6667A>T	XP_011529428.1:p.Lys2223Ter
NM_000132.4:c.6772A>T MANE Select	NP_000123.1:p.Lys2258Ter
NM_019863.3:c.367A>T	NP_063916.1:p.Lys123Ter