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Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.116832864A= , CM000673.2:g.116832864A=
GRCh38
NC_000011.9:g.116703580A= , CM000673.1:g.116703580A=
GRCh37
NC_000011.8:g.116208790A=
NCBI36
NG_008949.1:g.7957A=
Transcript Alleles
HGVS
Amino-acid Change
NM_000040.3:c.280A=
MANE Select
NP_000031.1:p.Thr94=
ENST00000227667.8:c.280A=
MANE Select
ENSP00000227667.2:p.Thr94=
NM_000040.1:c.280A=
NP_000031.1:p.Thr94=
NM_000040.2:c.280A=
NP_000031.1:p.Thr94=
ENST00000227667.7:c.280A=
ENSP00000227667.2:p.Thr94=
ENST00000375345.3:c.334A=
ENSP00000364494.1:p.Thr112=
ENST00000630701.1:c.334A=
ENSP00000486182.1:p.Thr112=