Canonical Allele Identifier: CA2695167708

Gene: F8

Linked Data

• gnomAD v4: X-154860367-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154860367G>T , CM000685.2:g.154860367G>T	GRCh38
NC_000023.10:g.154088642G>T , CM000685.1:g.154088642G>T	GRCh37
NC_000023.9:g.153741836G>T	NCBI36
NG_011403.1:g.167357C>A
NG_011403.2:g.167357C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6900+65C>A MANE Select	ENSP00000353393.4:n.6900+65C>A
ENST00000644698.1:c.633+65C>A	ENSP00000495706.1:n.633+65C>A
ENST00000330287.10:c.495+65C>A	ENSP00000327895.6:n.495+65C>A
ENST00000360256.8:c.6900+65C>A	ENSP00000353393.4:n.6900+65C>A
NM_000132.3:c.6900+65C>A	NP_000123.1:n.6900+65C>A
NM_019863.2:c.495+65C>A	NP_063916.1:n.495+65C>A
XM_011531126.1:c.6795+65C>A	XP_011529428.1:n.6795+65C>A
NM_000132.4:c.6900+65C>A MANE Select	NP_000123.1:n.6900+65C>A
NM_019863.3:c.495+65C>A	NP_063916.1:n.495+65C>A