Canonical Allele Identifier: CA2695170252

Gene: F8

Linked Data

• gnomAD v4: X-154997163-A-C

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.154997163A>C , CM000685.2:g.154997163A>C	GRCh38
NC_000023.10:g.154225438A>C , CM000685.1:g.154225438A>C	GRCh37
NC_000023.9:g.153878632A>C	NCBI36
NG_011403.1:g.30561T>G
NG_011403.2:g.30561T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000360256.9:c.266-68T>G MANE Select	ENSP00000353393.4:n.266-68T>G
ENST00000647125.1:c.*52-68T>G	ENSP00000496062.1:n.*52-68T>G
ENST00000360256.8:c.266-68T>G	ENSP00000353393.4:n.266-68T>G
ENST00000423959.5:c.161-68T>G	ENSP00000409446.1:n.161-68T>G
ENST00000453950.1:c.248-68T>G	ENSP00000389153.1:n.248-68T>G
NM_000132.3:c.266-68T>G	NP_000123.1:n.266-68T>G
XM_011531126.1:c.161-68T>G	XP_011529428.1:n.161-68T>G
NM_000132.4:c.266-68T>G MANE Select	NP_000123.1:n.266-68T>G