Canonical Allele Identifier: CA414920001
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154997034G>T , CM000685.2:g.154997034G>T GRCh38
NC_000023.10:g.154225309G>T , CM000685.1:g.154225309G>T GRCh37
NC_000023.9:g.153878503G>T NCBI36
NG_011403.1:g.30690C>A
NG_011403.2:g.30690C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.327C>A MANE Select ENSP00000353393.4:p.Asn109Lys
ENST00000647125.1:c.*113C>A ENSP00000496062.1:n.*113C>A
ENST00000360256.8:c.327C>A ENSP00000353393.4:p.Asn109Lys
ENST00000423959.5:c.222C>A ENSP00000409446.1:p.Asn74Lys
ENST00000453950.1:c.309C>A ENSP00000389153.1:p.Asn103Lys
NM_000132.3:c.327C>A NP_000123.1:p.Asn109Lys
XM_011531126.1:c.222C>A XP_011529428.1:p.Asn74Lys
NM_000132.4:c.327C>A MANE Select NP_000123.1:p.Asn109Lys