Canonical Allele Identifier: CA519367738
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154197799G>C (hg19)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154969524G>C , CM000685.2:g.154969524G>C GRCh38
NC_000023.10:g.154197799G>C , CM000685.1:g.154197799G>C GRCh37
NC_000023.9:g.153850993G>C NCBI36
NG_011403.1:g.58200C>G
NG_011403.2:g.58200C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.816C>G MANE Select ENSP00000353393.4:p.Val272=
ENST00000647125.1:c.*692C>G ENSP00000496062.1:n.*692C>G
ENST00000360256.8:c.816C>G ENSP00000353393.4:p.Val272=
NM_000132.3:c.816C>G NP_000123.1:p.Val272=
XM_011531126.1:c.711C>G XP_011529428.1:p.Val237=
NM_000132.4:c.816C>G MANE Select NP_000123.1:p.Val272=
Search 100 bp 5'
Search 100 bp 3'