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Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.86306310T= , CM000673.2:g.86306310T=
GRCh38
NC_000011.9:g.86017352T= , CM000673.1:g.86017352T=
GRCh37
NC_000011.8:g.85695000T=
NCBI36
NG_046865.1:g.9100T=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000278483.8:c.96T=
MANE Select
ENSP00000278483.3:p.Ser32=
ENST00000278483.7:c.96T=
ENSP00000278483.3:p.Ser32=
ENST00000528004.5:c.96T=
ENSP00000433815.1:p.Ser32=
ENST00000530208.1:n.171T=
ENST00000531485.5:n.236+3832T=
ENST00000532270.5:n.435T=
ENST00000533986.5:c.96T=
ENSP00000432699.1:p.Ser32=
NM_016401.3:c.96T=
NP_057485.2:p.Ser32=
NR_024596.1:n.171T=
NR_024597.1:n.268+3832T=
NR_024598.1:n.268+3832T=
XM_011545097.1:c.-22T=
XP_011543399.1:n.-22T=
XR_949963.1:n.319T=
NM_001322404.1:c.96T=
NP_001309333.1:p.Ser32=
NM_001322407.1:c.-22T=
NP_001309336.1:n.-22T=
NM_001322409.1:c.-22T=
NP_001309338.1:n.-22T=
NR_136324.1:n.318T=
XM_017017914.2:c.96T=
XP_016873403.1:p.Ser32=
XM_017017915.1:c.-22T=
XP_016873404.1:n.-22T=
XR_001747904.2:n.305T=
XR_949963.3:n.305T=
NM_016401.4:c.96T=
MANE Select
NP_057485.2:p.Ser32=
NM_001322404.2:c.96T=
NP_001309333.1:p.Ser32=
NM_001322407.2:c.-22T=
NP_001309336.1:n.-22T=
NM_001322409.2:c.-22T=
NP_001309338.1:n.-22T=
NR_024597.2:n.239+3832T=
NR_024598.2:n.239+3832T=
NR_136324.2:n.305T=