Canonical Allele Identifier: CA10567860
Gene: F8 HGNC NCBI

Linked Data

dbSNP Id: rs781907922
ExAC: X:154124358 G / A
gnomAD v2: X-154124358-G-A
gnomAD v4: X-154896083-G-A
MyVariant Identifiers: chrX:g.154124358G>A (hg19) chrX:g.154896083G>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154896083G>A , CM000685.2:g.154896083G>A GRCh38
NC_000023.10:g.154124358G>A , CM000685.1:g.154124358G>A GRCh37
NC_000023.9:g.153777552G>A NCBI36
NG_011403.1:g.131641C>T
NG_011403.2:g.131641C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6423C>T MANE Select ENSP00000353393.4:p.Thr2141=
ENST00000360256.8:c.6423C>T ENSP00000353393.4:p.Thr2141=
NM_000132.3:c.6423C>T NP_000123.1:p.Thr2141=
XM_011531126.1:c.6318C>T XP_011529428.1:p.Thr2106=
NM_000132.4:c.6423C>T MANE Select NP_000123.1:p.Thr2141=
Search 100 bp 5'
Search 100 bp 3'