Canonical Allele Identifier: CA645237059

Gene: F8

Linked Data

• dbSNP Id: rs1278743398
• gnomAD v2: X-154065867-C-T
• gnomAD v3: X-154837592-C-T
• gnomAD v4: X-154837592-C-T
• MyVariant Identifiers: chrX:g.154065867C>T (hg19) ; chrX:g.154837592C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837592C>T , CM000685.2:g.154837592C>T	GRCh38
NC_000023.10:g.154065867C>T , CM000685.1:g.154065867C>T	GRCh37
NC_000023.9:g.153719061C>T	NCBI36
NG_011403.1:g.190132G>A
NG_033065.1:g.2071G>A
NG_011403.2:g.190132G>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000360256.9:c.*5G>A MANE Select	ENSP00000353393.4:n.*5G>A
ENST00000644698.1:c.*5G>A	ENSP00000495706.1:n.*5G>A
ENST00000330287.10:c.*5G>A	ENSP00000327895.6:n.*5G>A
ENST00000360256.8:c.*5G>A	ENSP00000353393.4:n.*5G>A
NM_000132.3:c.*5G>A	NP_000123.1:n.*5G>A
NM_019863.2:c.*5G>A	NP_063916.1:n.*5G>A
XM_011531126.1:c.*5G>A	XP_011529428.1:n.*5G>A
NM_000132.4:c.*5G>A MANE Select	NP_000123.1:n.*5G>A
NM_019863.3:c.*5G>A	NP_063916.1:n.*5G>A