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Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.158645641G= , CM000665.2:g.158645641G=
GRCh38
NC_000003.11:g.158363430G= , CM000665.1:g.158363430G=
GRCh37
NC_000003.10:g.159846124G=
NCBI36
NG_008441.1:g.6114G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000486715.6:c.94G=
MANE Select
ENSP00000419038.1:p.Ala32=
ENST00000264263.9:c.94G=
ENSP00000264263.5:p.Ala32=
ENST00000464732.1:c.-132G=
ENSP00000417532.1:n.-132G=
ENST00000478254.5:c.94G=
ENSP00000417225.1:p.Ala32=
ENST00000478576.5:c.94G=
ENSP00000418755.1:p.Ala32=
ENST00000486715.5:c.94G=
ENSP00000419038.1:p.Ala32=
NM_001308164.1:c.94G=
NP_001295093.1:p.Ala32=
NM_001308166.1:c.94G=
NP_001295095.1:p.Ala32=
NM_024996.5:c.94G=
NP_079272.4:p.Ala32=
XM_006713795.1:c.94G=
XP_006713858.1:p.Ala32=
XM_006713795.2:c.94G=
XP_006713858.1:p.Ala32=
NM_001374355.1:c.94G=
NP_001361284.1:p.Ala32=
NM_001374356.1:c.94G=
NP_001361285.1:p.Ala32=
NM_001374357.1:c.-132G=
NP_001361286.1:n.-132G=
NM_001374358.1:c.94G=
NP_001361287.1:p.Ala32=
NM_001374359.1:c.-136G=
NP_001361288.1:n.-136G=
NM_001374360.1:c.-136G=
NP_001361289.1:n.-136G=
NM_001374361.1:c.-136G=
NP_001361290.1:n.-136G=
NM_024996.7:c.94G=
MANE Select
NP_079272.4:p.Ala32=
NR_164499.1:n.202G=
NR_164500.1:n.202G=
NR_164501.1:n.202G=
NR_164502.1:n.202G=
NM_001308164.2:c.94G=
NP_001295093.1:p.Ala32=
NM_001308166.2:c.94G=
NP_001295095.1:p.Ala32=