Canonical Allele Identifier: CA2695167278

Gene: F8

Linked Data

• gnomAD v4: X-154837403-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837403G>T , CM000685.2:g.154837403G>T	GRCh38
NC_000023.10:g.154065678G>T , CM000685.1:g.154065678G>T	GRCh37
NC_000023.9:g.153718872G>T	NCBI36
NG_011403.1:g.190321C>A
NG_033065.1:g.2260C>A
NG_011403.2:g.190321C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.*194C>A MANE Select	ENSP00000353393.4:n.*194C>A
ENST00000644698.1:c.*194C>A	ENSP00000495706.1:n.*194C>A
ENST00000330287.10:c.*194C>A	ENSP00000327895.6:n.*194C>A
ENST00000360256.8:c.*194C>A	ENSP00000353393.4:n.*194C>A
NM_000132.3:c.*194C>A	NP_000123.1:n.*194C>A
NM_019863.2:c.*194C>A	NP_063916.1:n.*194C>A
XM_011531126.1:c.*194C>A	XP_011529428.1:n.*194C>A
NM_000132.4:c.*194C>A MANE Select	NP_000123.1:n.*194C>A
NM_019863.3:c.*194C>A	NP_063916.1:n.*194C>A