Canonical Allele Identifier: CA414911782

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154185312T>G (hg19) ; chrX:g.154957037T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154957037T>G , CM000685.2:g.154957037T>G	GRCh38
NC_000023.10:g.154185312T>G , CM000685.1:g.154185312T>G	GRCh37
NC_000023.9:g.153838506T>G	NCBI36
NG_011403.1:g.70687A>C
NG_011403.2:g.70687A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.1672A>C MANE Select	ENSP00000353393.4:p.Met558Leu
ENST00000647125.1:c.*1548A>C	ENSP00000496062.1:n.*1548A>C
ENST00000360256.8:c.1672A>C	ENSP00000353393.4:p.Met558Leu
NM_000132.3:c.1672A>C	NP_000123.1:p.Met558Leu
XM_011531126.1:c.1567A>C	XP_011529428.1:p.Met523Leu
NM_000132.4:c.1672A>C MANE Select	NP_000123.1:p.Met558Leu