Canonical Allele Identifier: CA414897905
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154837748A>G , CM000685.2:g.154837748A>G GRCh38
NC_000023.10:g.154066023A>G , CM000685.1:g.154066023A>G GRCh37
NC_000023.9:g.153719217A>G NCBI36
NG_011403.1:g.189976T>C
NG_033065.1:g.1915T>C
NG_011403.2:g.189976T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.6905T>C MANE Select ENSP00000353393.4:p.Phe2302Ser
ENST00000644698.1:c.638T>C ENSP00000495706.1:p.Phe213Ser
ENST00000330287.10:c.500T>C ENSP00000327895.6:p.Phe167Ser
ENST00000360256.8:c.6905T>C ENSP00000353393.4:p.Phe2302Ser
NM_000132.3:c.6905T>C NP_000123.1:p.Phe2302Ser
NM_019863.2:c.500T>C NP_063916.1:p.Phe167Ser
XM_011531126.1:c.6800T>C XP_011529428.1:p.Phe2267Ser
NM_000132.4:c.6905T>C MANE Select NP_000123.1:p.Phe2302Ser
NM_019863.3:c.500T>C NP_063916.1:p.Phe167Ser