Canonical Allele Identifier: CA2695167268

Gene: F8

Linked Data

• gnomAD v4: X-154837394-T-G

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837394T>G , CM000685.2:g.154837394T>G	GRCh38
NC_000023.10:g.154065669T>G , CM000685.1:g.154065669T>G	GRCh37
NC_000023.9:g.153718863T>G	NCBI36
NG_011403.1:g.190330A>C
NG_033065.1:g.2269A>C
NG_011403.2:g.190330A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.*203A>C MANE Select	ENSP00000353393.4:n.*203A>C
ENST00000644698.1:c.*203A>C	ENSP00000495706.1:n.*203A>C
ENST00000330287.10:c.*203A>C	ENSP00000327895.6:n.*203A>C
ENST00000360256.8:c.*203A>C	ENSP00000353393.4:n.*203A>C
NM_000132.3:c.*203A>C	NP_000123.1:n.*203A>C
NM_019863.2:c.*203A>C	NP_063916.1:n.*203A>C
XM_011531126.1:c.*203A>C	XP_011529428.1:n.*203A>C
NM_000132.4:c.*203A>C MANE Select	NP_000123.1:n.*203A>C
NM_019863.3:c.*203A>C	NP_063916.1:n.*203A>C