Canonical Allele Identifier: CA414906126
Gene: F8 HGNC NCBI

Linked Data

MyVariant Identifiers: chrX:g.154132281C>G (hg19) chrX:g.154904006C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154904006C>G , CM000685.2:g.154904006C>G GRCh38
NC_000023.10:g.154132281C>G , CM000685.1:g.154132281C>G GRCh37
NC_000023.9:g.153785475C>G NCBI36
NG_011403.1:g.123718G>C
NG_011403.2:g.123718G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.5898G>C MANE Select ENSP00000353393.4:p.Met1966Ile
ENST00000360256.8:c.5898G>C ENSP00000353393.4:p.Met1966Ile
NM_000132.3:c.5898G>C NP_000123.1:p.Met1966Ile
XM_011531126.1:c.5793G>C XP_011529428.1:p.Met1931Ile
NM_000132.4:c.5898G>C MANE Select NP_000123.1:p.Met1966Ile
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