Canonical Allele Identifier: CA414906461

Gene: F8

Linked Data

• MyVariant Identifiers: chrX:g.154132322T>G (hg19) ; chrX:g.154904047T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154904047T>G , CM000685.2:g.154904047T>G	GRCh38
NC_000023.10:g.154132322T>G , CM000685.1:g.154132322T>G	GRCh37
NC_000023.9:g.153785516T>G	NCBI36
NG_011403.1:g.123677A>C
NG_011403.2:g.123677A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.5857A>C MANE Select	ENSP00000353393.4:p.Met1953Leu
ENST00000360256.8:c.5857A>C	ENSP00000353393.4:p.Met1953Leu
NM_000132.3:c.5857A>C	NP_000123.1:p.Met1953Leu
XM_011531126.1:c.5752A>C	XP_011529428.1:p.Met1918Leu
NM_000132.4:c.5857A>C MANE Select	NP_000123.1:p.Met1953Leu