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Genomic Alleles
HGVS
Genome Assembly
NC_000007.14:g.83981425C= , CM000669.2:g.83981425C=
GRCh38
NC_000007.13:g.83610741C= , CM000669.1:g.83610741C=
GRCh37
NC_000007.12:g.83448677C=
NCBI36
NG_011489.1:g.218477G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000265362.9:c.1548G=
MANE Select
ENSP00000265362.3:p.Arg516=
ENST00000265362.8:c.1548G=
ENSP00000265362.3:p.Arg516=
ENST00000436949.5:c.1548G=
ENSP00000415260.1:p.Arg516=
NM_006080.2:c.1548G=
NP_006071.1:p.Arg516=
XM_005250110.2:c.1548G=
XP_005250167.1:p.Arg516=
XM_005250111.3:c.1548G=
XP_005250168.1:p.Arg516=
XM_006715839.2:c.1548G=
XP_006715902.1:p.Arg516=
XM_011515734.1:c.1548G=
XP_011514036.1:p.Arg516=
XM_011515735.1:c.1548G=
XP_011514037.1:p.Arg516=
XM_005250110.3:c.1548G=
XP_005250167.1:p.Arg516=
XM_005250111.4:c.1548G=
XP_005250168.1:p.Arg516=
XM_006715839.3:c.1548G=
XP_006715902.1:p.Arg516=
XM_011515734.3:c.1548G=
XP_011514036.1:p.Arg516=
XM_017011673.1:c.1548G=
XP_016867162.1:p.Arg516=
XM_024446633.1:c.1548G=
XP_024302401.1:p.Arg516=
NM_006080.3:c.1548G=
MANE Select
NP_006071.1:p.Arg516=