Canonical Allele Identifier: CA519357755
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154182234G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154953959G>C , CM000685.2:g.154953959G>C GRCh38
NC_000023.10:g.154182234G>C , CM000685.1:g.154182234G>C GRCh37
NC_000023.9:g.153835428G>C NCBI36
NG_011403.1:g.73765C>G
NG_011403.2:g.73765C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1836C>G MANE Select ENSP00000353393.4:p.Arg612=
ENST00000647125.1:c.*1712C>G ENSP00000496062.1:n.*1712C>G
ENST00000360256.8:c.1836C>G ENSP00000353393.4:p.Arg612=
NM_000132.3:c.1836C>G NP_000123.1:p.Arg612=
XM_011531126.1:c.1731C>G XP_011529428.1:p.Arg577=
NM_000132.4:c.1836C>G MANE Select NP_000123.1:p.Arg612=
Search 100 bp 5'
Search 100 bp 3'