Canonical Allele Identifier: CA414907370

Gene: F8

Linked Data

• gnomAD v4: X-154863143-G-T
• MyVariant Identifiers: chrX:g.154091418G>T (hg19) ; chrX:g.154863143G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154863143G>T , CM000685.2:g.154863143G>T	GRCh38
NC_000023.10:g.154091418G>T , CM000685.1:g.154091418G>T	GRCh37
NC_000023.9:g.153744612G>T	NCBI36
NG_011403.1:g.164581C>A
NG_011403.2:g.164581C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.6514C>A MANE Select	ENSP00000353393.4:p.Pro2172Thr
ENST00000644698.1:c.247C>A	ENSP00000495706.1:p.Pro83Thr
ENST00000330287.10:c.109C>A	ENSP00000327895.6:p.Pro37Thr
ENST00000360256.8:c.6514C>A	ENSP00000353393.4:p.Pro2172Thr
NM_000132.3:c.6514C>A	NP_000123.1:p.Pro2172Thr
NM_019863.2:c.109C>A	NP_063916.1:p.Pro37Thr
XM_011531126.1:c.6409C>A	XP_011529428.1:p.Pro2137Thr
NM_000132.4:c.6514C>A MANE Select	NP_000123.1:p.Pro2172Thr
NM_019863.3:c.109C>A	NP_063916.1:p.Pro37Thr