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Genomic Alleles
HGVS
Genome Assembly
NC_000009.12:g.137232605T= , CM000671.2:g.137232605T=
GRCh38
NC_000009.11:g.140127057T= , CM000671.1:g.140127057T=
GRCh37
NC_000009.10:g.139246878T=
NCBI36
NG_017008.1:g.6849T=
NG_017008.2:g.6705T=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000673835.1:c.206T=
MANE Select
ENSP00000501114.1:p.Val69=
ENST00000673865.1:c.206T=
ENSP00000501101.1:p.Val69=
ENST00000673953.1:c.206T=
ENSP00000501108.1:p.Val69=
ENST00000361134.2:c.206T=
ENSP00000355353.2:p.Val69=
ENST00000538474.5:c.206T=
ENSP00000442397.1:p.Val69=
NM_001177316.1:c.206T=
NP_001170787.1:p.Val69=
NM_001177317.1:c.206T=
NP_001170788.1:p.Val69=
NM_080877.2:c.206T=
NP_543153.1:p.Val69=
XM_011518256.1:c.206T=
XP_011516558.1:p.Val69=
XM_011518257.1:c.206T=
XP_011516559.1:p.Val69=
XM_011518258.1:c.206T=
XP_011516560.1:p.Val69=
XM_011518259.1:c.206T=
XP_011516561.1:p.Val69=
XM_011518260.1:c.206T=
XP_011516562.1:p.Val69=
XM_011518261.1:c.206T=
XP_011516563.1:p.Val69=
XM_011518262.1:c.206T=
XP_011516564.1:p.Val69=
XM_011518257.2:c.206T=
XP_011516559.1:p.Val69=
XM_011518261.2:c.206T=
XP_011516563.1:p.Val69=
XM_017014290.1:c.206T=
XP_016869779.1:p.Val69=
XM_017014291.1:c.206T=
XP_016869780.1:p.Val69=
XM_017014292.1:c.206T=
XP_016869781.1:p.Val69=
NM_001177316.2:c.206T=
MANE Select
NP_001170787.2:p.Val69=
NM_001177317.2:c.206T=
NP_001170788.2:p.Val69=
NM_080877.3:c.206T=
NP_543153.2:p.Val69=