Canonical Allele Identifier: CA645237040

Gene: F8

Linked Data

• dbSNP Id: rs1557270991
• gnomAD v2: X-154065672-G-A
• gnomAD v3: X-154837397-G-A
• gnomAD v4: X-154837397-G-A
• MyVariant Identifiers: chrX:g.154065672G>A (hg19) ; chrX:g.154837397G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154837397G>A , CM000685.2:g.154837397G>A	GRCh38
NC_000023.10:g.154065672G>A , CM000685.1:g.154065672G>A	GRCh37
NC_000023.9:g.153718866G>A	NCBI36
NG_011403.1:g.190327C>T
NG_033065.1:g.2266C>T
NG_011403.2:g.190327C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.*200C>T MANE Select	ENSP00000353393.4:n.*200C>T
ENST00000644698.1:c.*200C>T	ENSP00000495706.1:n.*200C>T
ENST00000330287.10:c.*200C>T	ENSP00000327895.6:n.*200C>T
ENST00000360256.8:c.*200C>T	ENSP00000353393.4:n.*200C>T
NM_000132.3:c.*200C>T	NP_000123.1:n.*200C>T
NM_019863.2:c.*200C>T	NP_063916.1:n.*200C>T
XM_011531126.1:c.*200C>T	XP_011529428.1:n.*200C>T
NM_000132.4:c.*200C>T MANE Select	NP_000123.1:n.*200C>T
NM_019863.3:c.*200C>T	NP_063916.1:n.*200C>T