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Genomic Alleles
HGVS
Genome Assembly
NC_000020.11:g.46725758T= , CM000682.2:g.46725758T=
GRCh38
NC_000020.10:g.45354397T= , CM000682.1:g.45354397T=
GRCh37
NC_000020.9:g.44787804T=
NCBI36
NG_016284.1:g.21119T=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000359271.4:c.722T=
MANE Select
ENSP00000352216.2:p.Phe241=
ENST00000359271.3:c.722T=
ENSP00000352216.2:p.Phe241=
NM_030777.3:c.722T=
NP_110404.1:p.Phe241=
XM_011529060.1:c.785T=
XP_011527362.1:p.Phe262=
XM_011529061.1:c.731T=
XP_011527363.1:p.Phe244=
XM_011529062.1:c.785T=
XP_011527364.1:p.Phe262=
XM_011529063.1:c.785T=
XP_011527365.1:p.Phe262=
XM_011529064.1:c.785T=
XP_011527366.1:p.Phe262=
XM_011529065.1:c.785T=
XP_011527367.1:p.Phe262=
XR_936641.1:n.921T=
XM_011529060.2:c.785T=
XP_011527362.1:p.Phe262=
XM_011529061.2:c.731T=
XP_011527363.1:p.Phe244=
XM_011529062.2:c.785T=
XP_011527364.1:p.Phe262=
XM_011529063.2:c.785T=
XP_011527365.1:p.Phe262=
XM_011529064.2:c.785T=
XP_011527366.1:p.Phe262=
XM_011529065.2:c.785T=
XP_011527367.1:p.Phe262=
XM_017028087.2:c.722T=
XP_016883576.1:p.Phe241=
XR_936641.2:n.908T=
NM_030777.4:c.722T=
MANE Select
NP_110404.1:p.Phe241=