Canonical Allele Identifier: CA519358215
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154185238T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154956963T>C , CM000685.2:g.154956963T>C GRCh38
NC_000023.10:g.154185238T>C , CM000685.1:g.154185238T>C GRCh37
NC_000023.9:g.153838432T>C NCBI36
NG_011403.1:g.70761A>G
NG_011403.2:g.70761A>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1746A>G MANE Select ENSP00000353393.4:p.Gly582=
ENST00000647125.1:c.*1622A>G ENSP00000496062.1:n.*1622A>G
ENST00000360256.8:c.1746A>G ENSP00000353393.4:p.Gly582=
NM_000132.3:c.1746A>G NP_000123.1:p.Gly582=
XM_011531126.1:c.1641A>G XP_011529428.1:p.Gly547=
NM_000132.4:c.1746A>G MANE Select NP_000123.1:p.Gly582=