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Genomic Alleles
HGVS
Genome Assembly
NC_000021.9:g.18281061C= , CM000683.2:g.18281061C=
GRCh38
NC_000021.8:g.19653378C= , CM000683.1:g.19653378C=
GRCh37
NC_000021.7:g.18575249C=
NCBI36
NG_012207.1:g.127593G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000284885.8:c.2647G=
MANE Select
ENSP00000284885.3:p.Glu883=
ENST00000284885.7:c.2647G=
ENSP00000284885.3:p.Glu883=
NM_002772.2:c.2647G=
NP_002763.2:p.Glu883=
XM_011529654.1:c.2782G=
XP_011527956.1:p.Glu928=
XM_011529655.1:c.2782G=
XP_011527957.1:p.Glu928=
XM_011529656.1:c.2782G=
XP_011527958.1:p.Glu928=
XM_011529657.1:c.2737G=
XP_011527959.1:p.Glu913=
XM_011529658.1:c.2701G=
XP_011527960.1:p.Glu901=
XM_011529659.1:c.2692G=
XP_011527961.1:p.Glu898=
XM_011529654.2:c.2782G=
XP_011527956.1:p.Glu928=
XM_011529656.2:c.2782G=
XP_011527958.1:p.Glu928=
XM_011529657.2:c.2737G=
XP_011527959.1:p.Glu913=
XM_011529658.2:c.2701G=
XP_011527960.1:p.Glu901=
NM_002772.3:c.2647G=
MANE Select
NP_002763.3:p.Glu883=