Canonical Allele Identifier: CA414914728
Gene: F8 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.154966047T>G , CM000685.2:g.154966047T>G GRCh38
NC_000023.10:g.154194322T>G , CM000685.1:g.154194322T>G GRCh37
NC_000023.9:g.153847516T>G NCBI36
NG_011403.1:g.61677A>C
NG_011403.2:g.61677A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000360256.9:c.1366A>C MANE Select ENSP00000353393.4:p.Lys456Gln
ENST00000647125.1:c.*1242A>C ENSP00000496062.1:n.*1242A>C
ENST00000360256.8:c.1366A>C ENSP00000353393.4:p.Lys456Gln
ENST00000483822.2:n.186A>C
NM_000132.3:c.1366A>C NP_000123.1:p.Lys456Gln
XM_011531126.1:c.1261A>C XP_011529428.1:p.Lys421Gln
NM_000132.4:c.1366A>C MANE Select NP_000123.1:p.Lys456Gln