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Genomic Alleles
HGVS
Genome Assembly
NC_000004.12:g.23814276C= , CM000666.2:g.23814276C=
GRCh38
NC_000004.11:g.23815899C= , CM000666.1:g.23815899C=
GRCh37
NC_000004.10:g.23424997C=
NCBI36
NG_028250.1:g.80802G=
NG_028250.2:g.663700G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000264867.7:c.1207G=
MANE Select
ENSP00000264867.2:p.Glu403=
ENST00000264867.6:c.1207G=
ENSP00000264867.2:p.Glu403=
ENST00000506055.5:c.*422G=
ENSP00000423075.1:n.*422G=
ENST00000509702.5:n.1247G=
ENST00000613098.4:c.826G=
ENSP00000481498.1:p.Glu276=
NM_013261.3:c.1207G=
NP_037393.1:p.Glu403=
XM_005248130.2:c.1222G=
XP_005248187.1:p.Glu408=
XM_005248131.3:c.1219G=
XP_005248188.1:p.Glu407=
XM_005248132.1:c.1198G=
XP_005248189.1:p.Glu400=
XM_005248134.3:c.1222G=
XP_005248191.1:p.Glu408=
XM_011513764.1:c.1207G=
XP_011512066.1:p.Glu403=
XM_011513765.1:c.1171G=
XP_011512067.1:p.Glu391=
XM_011513766.1:c.1102G=
XP_011512068.1:p.Glu368=
XM_011513767.1:c.1102G=
XP_011512069.1:p.Glu368=
XM_011513768.1:c.1102G=
XP_011512070.1:p.Glu368=
XM_011513769.1:c.1222G=
XP_011512071.1:p.Glu408=
XM_011513770.1:c.826G=
XP_011512072.1:p.Glu276=
XM_011513771.1:c.826G=
XP_011512073.1:p.Glu276=
NM_001330751.1:c.1222G=
NP_001317680.1:p.Glu408=
NM_001330752.1:c.1171G=
NP_001317681.1:p.Glu391=
NM_001330753.1:c.826G=
NP_001317682.1:p.Glu276=
NM_001354825.1:c.1222G=
NP_001341754.1:p.Glu408=
NM_001354826.1:c.826G=
NP_001341755.1:p.Glu276=
NM_001354827.1:c.1222G=
NP_001341756.1:p.Glu408=
NM_013261.4:c.1207G=
NP_037393.1:p.Glu403=
NR_148981.1:n.1734G=
NR_148982.1:n.1807G=
NR_148983.1:n.1960G=
NR_148984.1:n.1358G=
NR_148985.1:n.1872G=
NR_148986.1:n.1877G=
NR_148987.1:n.1959G=
XM_005248131.5:c.1219G=
XP_005248188.1:p.Glu407=
XM_005248134.4:c.1222G=
XP_005248191.1:p.Glu408=
XM_011513769.2:c.1222G=
XP_011512071.1:p.Glu408=
XM_024453878.1:c.1222G=
XP_024309646.1:p.Glu408=
NM_013261.5:c.1207G=
MANE Select
NP_037393.1:p.Glu403=
NM_001330751.2:c.1222G=
NP_001317680.1:p.Glu408=
NM_001330752.2:c.1171G=
NP_001317681.1:p.Glu391=
NM_001354825.2:c.1222G=
NP_001341754.1:p.Glu408=
NM_001354826.2:c.826G=
NP_001341755.1:p.Glu276=
NM_001354827.2:c.1222G=
NP_001341756.1:p.Glu408=
NR_148981.2:n.1810G=
NR_148982.2:n.1883G=
NR_148983.2:n.2036G=
NR_148984.2:n.1328G=
NR_148985.2:n.1948G=
NR_148986.2:n.1953G=
NR_148987.2:n.2035G=
NM_001330753.2:c.826G=
NP_001317682.1:p.Glu276=