Canonical Allele Identifier: CA519355203

Gene: F8

Linked Data

• COSMIC: COSM3844129 ; COSM3844130
• MyVariant Identifiers: chrX:g.154065914C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837639C>G , CM000685.2:g.154837639C>G	GRCh38
NC_000023.10:g.154065914C>G , CM000685.1:g.154065914C>G	GRCh37
NC_000023.9:g.153719108C>G	NCBI36
NG_011403.1:g.190085G>C
NG_033065.1:g.2024G>C
NG_011403.2:g.190085G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.7014G>C MANE Select	ENSP00000353393.4:p.Leu2338=
ENST00000644698.1:c.747G>C	ENSP00000495706.1:p.Leu249=
ENST00000330287.10:c.609G>C	ENSP00000327895.6:p.Leu203=
ENST00000360256.8:c.7014G>C	ENSP00000353393.4:p.Leu2338=
NM_000132.3:c.7014G>C	NP_000123.1:p.Leu2338=
NM_019863.2:c.609G>C	NP_063916.1:p.Leu203=
XM_011531126.1:c.6909G>C	XP_011529428.1:p.Leu2303=
NM_000132.4:c.7014G>C MANE Select	NP_000123.1:p.Leu2338=
NM_019863.3:c.609G>C	NP_063916.1:p.Leu203=