Canonical Allele Identifier: CA414445888
Gene: F9 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.139561785T>C , CM000685.2:g.139561785T>C GRCh38
NC_000023.10:g.138643944T>C , CM000685.1:g.138643944T>C GRCh37
NC_000023.9:g.138471610T>C NCBI36
NG_007994.1:g.36050T>C , LRG_556:g.36050T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000218099.7:c.1100T>C MANE Select ENSP00000218099.2:p.Leu367Ser
ENST00000643157.1:n.1723+44T>C
ENST00000218099.6:c.1100T>C ENSP00000218099.2:p.Leu367Ser
ENST00000394090.2:c.986T>C ENSP00000377650.2:p.Leu329Ser
NM_000133.3:c.1100T>C , LRG_556t1:c.1100T>C NP_000124.1:p.Leu367Ser
NM_001313913.1:c.986T>C NP_001300842.1:p.Leu329Ser
XM_005262397.3:c.971T>C XP_005262454.1:p.Leu324Ser
XM_005262397.4:c.971T>C XP_005262454.1:p.Leu324Ser
NM_000133.4:c.1100T>C MANE Select NP_000124.1:p.Leu367Ser
NM_001313913.2:c.986T>C NP_001300842.1:p.Leu329Ser