Canonical Allele Identifier: CA414906792
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154863084A>C , CM000685.2:g.154863084A>C GRCh38
NC_000023.10:g.154091359A>C , CM000685.1:g.154091359A>C GRCh37
NC_000023.9:g.153744553A>C NCBI36
NG_011403.1:g.164640T>G
NG_011403.2:g.164640T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6573T>G MANE Select ENSP00000353393.4:p.Asn2191Lys
ENST00000644698.1:c.306T>G ENSP00000495706.1:p.Asn102Lys
ENST00000330287.10:c.168T>G ENSP00000327895.6:p.Asn56Lys
ENST00000360256.8:c.6573T>G ENSP00000353393.4:p.Asn2191Lys
NM_000132.3:c.6573T>G NP_000123.1:p.Asn2191Lys
NM_019863.2:c.168T>G NP_063916.1:p.Asn56Lys
XM_011531126.1:c.6468T>G XP_011529428.1:p.Asn2156Lys
NM_000132.4:c.6573T>G MANE Select NP_000123.1:p.Asn2191Lys
NM_019863.3:c.168T>G NP_063916.1:p.Asn56Lys