Canonical Allele Identifier: CA414902986
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154860447C>G , CM000685.2:g.154860447C>G GRCh38
NC_000023.10:g.154088722C>G , CM000685.1:g.154088722C>G GRCh37
NC_000023.9:g.153741916C>G NCBI36
NG_011403.1:g.167277G>C
NG_011403.2:g.167277G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000360256.9:c.6885G>C MANE Select ENSP00000353393.4:p.Gln2295His
ENST00000644698.1:c.618G>C ENSP00000495706.1:p.Gln206His
ENST00000330287.10:c.480G>C ENSP00000327895.6:p.Gln160His
ENST00000360256.8:c.6885G>C ENSP00000353393.4:p.Gln2295His
NM_000132.3:c.6885G>C NP_000123.1:p.Gln2295His
NM_019863.2:c.480G>C NP_063916.1:p.Gln160His
XM_011531126.1:c.6780G>C XP_011529428.1:p.Gln2260His
NM_000132.4:c.6885G>C MANE Select NP_000123.1:p.Gln2295His
NM_019863.3:c.480G>C NP_063916.1:p.Gln160His