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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.173914868G>C , CM000663.2:g.173914868G>C
GRCh38
NC_000001.10:g.173884006G>C , CM000663.1:g.173884006G>C
GRCh37
NC_000001.9:g.172150629G>C
NCBI36
NG_012462.1:g.7511C>G , LRG_577:g.7511C>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000367698.4:c.93C>G
MANE Select
ENSP00000356671.3:p.Thr31=
ENST00000367698.3:c.93C>G
ENSP00000356671.3:p.Thr31=
ENST00000494024.1:n.319C>G
ENST00000617423.4:c.93C>G
ENSP00000478688.1:p.Thr31=
NM_000488.3:c.93C>G , LRG_577t1:c.93C>G
NP_000479.1:p.Thr31=
XM_005245198.2:c.-52C>G
XP_005245255.1:n.-52C>G
NM_001365052.1:c.-52C>G
NP_001351981.1:n.-52C>G
NM_000488.4:c.93C>G
MANE Select
NP_000479.1:p.Thr31=
NM_001365052.2:c.-52C>G
NP_001351981.1:n.-52C>G
NM_001386302.1:c.93C>G
NP_001373231.1:p.Thr31=
NM_001386303.1:c.174C>G
NP_001373232.1:p.Thr58=
NM_001386304.1:c.93C>G
NP_001373233.1:p.Thr31=
NM_001386305.1:c.93C>G
NP_001373234.1:p.Thr31=
NM_001386306.1:c.93C>G
NP_001373235.1:p.Thr31=