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Genomic Alleles
HGVS
Genome Assembly
NC_000023.11:g.85963749G>A , CM000685.2:g.85963749G>A
GRCh38
NC_000023.10:g.85218754G>A , CM000685.1:g.85218754G>A
GRCh37
NC_000023.9:g.85105410G>A
NCBI36
NG_009874.2:g.88814C>T , LRG_699:g.88814C>T
Transcript Alleles
HGVS
Amino-acid Change
ENST00000357749.7:c.618C>T
MANE Select
ENSP00000350386.2:p.Thr206=
ENST00000357749.6:c.618C>T
ENSP00000350386.2:p.Thr206=
ENST00000467744.2:n.126+63742C>T
NM_000390.2:c.618C>T , LRG_699t1:c.618C>T
NP_000381.1:p.Thr206=
XM_006724615.2:c.555C>T
XP_006724678.1:p.Thr185=
XM_011530839.1:c.174C>T
XP_011529141.1:p.Thr58=
NM_000390.3:c.618C>T
NP_000381.1:p.Thr206=
NM_001320959.1:c.174C>T
NP_001307888.1:p.Thr58=
NM_001362517.1:c.174C>T
NP_001349446.1:p.Thr58=
NM_001362518.1:c.174C>T
NP_001349447.1:p.Thr58=
NM_001362519.1:c.174C>T
NP_001349448.1:p.Thr58=
XM_017029242.2:c.618C>T
XP_016884731.1:p.Thr206=
XM_017029246.1:c.174C>T
XP_016884735.1:p.Thr58=
XM_024452331.1:c.174C>T
XP_024308099.1:p.Thr58=
NM_000390.4:c.618C>T
MANE Select
NP_000381.1:p.Thr206=
NM_001362518.2:c.174C>T
NP_001349447.1:p.Thr58=