Canonical Allele Identifier: CA414911617
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154185240C>A (hg19) chrX:g.154956965C>A (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154956965C>A , CM000685.2:g.154956965C>A GRCh38
NC_000023.10:g.154185240C>A , CM000685.1:g.154185240C>A GRCh37
NC_000023.9:g.153838434C>A NCBI36
NG_011403.1:g.70759G>T
NG_011403.2:g.70759G>T

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.1744G>T MANE Select ENSP00000353393.4:p.Gly582Ter
ENST00000647125.1:c.*1620G>T ENSP00000496062.1:n.*1620G>T
ENST00000360256.8:c.1744G>T ENSP00000353393.4:p.Gly582Ter
NM_000132.3:c.1744G>T NP_000123.1:p.Gly582Ter
XM_011531126.1:c.1639G>T XP_011529428.1:p.Gly547Ter
NM_000132.4:c.1744G>T MANE Select NP_000123.1:p.Gly582Ter
Search 100 bp 5'
Search 100 bp 3'