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Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.39244490A>G , CM000666.2:g.39244490A>G
GRCh38
NC_000004.11:g.39246110A>G , CM000666.1:g.39246110A>G
GRCh37
NC_000004.10:g.38922505A>G
NCBI36
NG_031813.1:g.67087A>G
Transcript Alleles
HGVS
Amino-acid Change
ENST00000399820.8:c.2583A>G
MANE Select
ENSP00000382717.3:p.Gln861=
ENST00000399820.7:c.2583A>G
ENSP00000382717.3:p.Gln861=
ENST00000506869.5:c.*2164A>G
ENSP00000424319.1:n.*2164A>G
ENST00000512095.5:n.1581A>G
NM_025132.3:c.2583A>G
NP_079408.3:p.Gln861=
XM_011513724.1:c.2595A>G
XP_011512026.1:p.Gln865=
XM_011513725.1:c.2529A>G
XP_011512027.1:p.Gln843=
XM_011513726.1:c.2115A>G
XP_011512028.1:p.Gln705=
XM_011513727.1:c.2115A>G
XP_011512029.1:p.Gln705=
XM_011513728.1:c.2103A>G
XP_011512030.1:p.Gln701=
XM_011513729.1:c.2595A>G
XP_011512031.1:p.Gln865=
XR_925155.1:n.2659A>G
NM_001317924.1:c.2103A>G
NP_001304853.1:p.Gln701=
XM_011513725.2:c.2529A>G
XP_011512027.1:p.Gln843=
XM_011513726.3:c.2115A>G
XP_011512028.1:p.Gln705=
XM_017008501.1:c.2103A>G
XP_016863990.1:p.Gln701=
XR_001741306.1:n.2659A>G
XR_001741307.1:n.2647A>G
XR_001741308.1:n.2659A>G
XR_001741309.1:n.2647A>G
XR_001741310.1:n.2647A>G
XR_001741311.2:n.2496A>G
NM_025132.4:c.2583A>G
MANE Select
NP_079408.3:p.Gln861=
NM_001317924.2:c.2103A>G
NP_001304853.1:p.Gln701=