Canonical Allele Identifier: CA414907847

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154091469T>G (hg19) ; chrX:g.154863194T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863194T>G , CM000685.2:g.154863194T>G	GRCh38
NC_000023.10:g.154091469T>G , CM000685.1:g.154091469T>G	GRCh37
NC_000023.9:g.153744663T>G	NCBI36
NG_011403.1:g.164530A>C
NG_011403.2:g.164530A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6463A>C MANE Select	ENSP00000353393.4:p.Lys2155Gln
ENST00000644698.1:c.196A>C	ENSP00000495706.1:p.Lys66Gln
ENST00000330287.10:c.58A>C	ENSP00000327895.6:p.Lys20Gln
ENST00000360256.8:c.6463A>C	ENSP00000353393.4:p.Lys2155Gln
NM_000132.3:c.6463A>C	NP_000123.1:p.Lys2155Gln
NM_019863.2:c.58A>C	NP_063916.1:p.Lys20Gln
XM_011531126.1:c.6358A>C	XP_011529428.1:p.Lys2120Gln
NM_000132.4:c.6463A>C MANE Select	NP_000123.1:p.Lys2155Gln
NM_019863.3:c.58A>C	NP_063916.1:p.Lys20Gln