Canonical Allele Identifier: CA337319320

Gene: F8

Linked Data

• dbSNP Id: rs978734391
• MyVariant Identifiers: chrX:g.154837504A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837504A>G , CM000685.2:g.154837504A>G	GRCh38
NC_000023.10:g.154065779A>G , CM000685.1:g.154065779A>G	GRCh37
NC_000023.9:g.153718973A>G	NCBI36
NG_011403.1:g.190220T>C
NG_033065.1:g.2159T>C
NG_011403.2:g.190220T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.*93T>C MANE Select	ENSP00000353393.4:n.*93T>C
ENST00000644698.1:c.*93T>C	ENSP00000495706.1:n.*93T>C
ENST00000330287.10:c.*93T>C	ENSP00000327895.6:n.*93T>C
ENST00000360256.8:c.*93T>C	ENSP00000353393.4:n.*93T>C
NM_000132.3:c.*93T>C	NP_000123.1:n.*93T>C
NM_019863.2:c.*93T>C	NP_063916.1:n.*93T>C
XM_011531126.1:c.*93T>C	XP_011529428.1:n.*93T>C
NM_000132.4:c.*93T>C MANE Select	NP_000123.1:n.*93T>C
NM_019863.3:c.*93T>C	NP_063916.1:n.*93T>C