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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.12192929C>G , CM000663.2:g.12192929C>G
GRCh38
NC_000001.10:g.12252986C>G , CM000663.1:g.12252986C>G
GRCh37
NC_000001.9:g.12175573C>G
NCBI36
NG_029791.1:g.30927C>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000376259.7:c.618C>G
MANE Select
ENSP00000365435.3:p.Thr206=
ENST00000376259.6:c.618C>G
ENSP00000365435.3:p.Thr206=
ENST00000489921.1:n.330C>G
ENST00000492361.1:n.607C>G
NM_001066.2:c.618C>G
NP_001057.1:p.Thr206=
XM_011542060.1:c.618C>G
XP_011540362.1:p.Thr206=
XM_011542061.1:c.618C>G
XP_011540363.1:p.Thr206=
XM_011542062.1:c.597C>G
XP_011540364.1:p.Thr199=
XM_011542063.1:c.618C>G
XP_011540365.1:p.Thr206=
XM_011542060.2:c.618C>G
XP_011540362.1:p.Thr206=
XM_011542063.2:c.618C>G
XP_011540365.1:p.Thr206=
XM_017002211.1:c.618C>G
XP_016857700.1:p.Thr206=
XM_017002214.1:c.33C>G
XP_016857703.1:p.Thr11=
XM_017002215.1:c.33C>G
XP_016857704.1:p.Thr11=
NM_001066.3:c.618C>G
MANE Select
NP_001057.1:p.Thr206=