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Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.25234271C= , CM000664.2:g.25234271C=
GRCh38
NC_000002.11:g.25457140C= , CM000664.1:g.25457140C=
GRCh37
NC_000002.10:g.25310644C=
NCBI36
NG_029465.2:g.113320G= , LRG_459:g.113320G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000683393.1:c.1893G=
ENSP00000508654.1:n.1893G=
ENST00000683760.1:c.*8G=
ENSP00000507765.1:n.*8G=
ENST00000321117.10:c.*8G=
MANE Select
ENSP00000324375.5:n.*8G=
ENST00000264709.7:c.*8G=
ENSP00000264709.3:n.*8G=
ENST00000321117.9:c.*8G=
ENSP00000324375.5:n.*8G=
ENST00000380746.8:c.*8G=
ENSP00000370122.4:n.*8G=
ENST00000380756.7:c.*600G=
ENSP00000370132.3:n.*600G=
ENST00000402667.1:c.*8G=
ENSP00000384237.1:n.*8G=
NM_022552.4:c.*8G= , LRG_459t1:c.*8G=
NP_072046.2:n.*8G=
NM_153759.3:c.*8G= , LRG_459t2:c.*8G=
NP_715640.2:n.*8G=
NM_175629.2:c.*8G= , LRG_459t4:c.*8G=
NP_783328.1:n.*8G=
XM_005264175.3:c.*8G=
XP_005264232.1:n.*8G=
XM_005264177.3:c.*8G=
XP_005264234.1:n.*8G=
XM_006711958.2:c.*8G=
XP_006712021.1:n.*8G=
XM_011532662.1:c.*8G=
XP_011530964.1:n.*8G=
XM_011532663.1:c.*8G=
XP_011530965.1:n.*8G=
XM_011532665.1:c.*8G=
XP_011530967.1:n.*8G=
XM_011532666.1:c.*8G=
XP_011530968.1:n.*8G=
XM_011532667.1:c.*8G=
XP_011530969.1:n.*8G=
NM_001320893.1:c.*8G=
NP_001307822.1:n.*8G=
NR_135490.1:n.3284G=
XM_005264175.5:c.*8G=
XP_005264232.1:n.*8G=
XM_005264177.4:c.*8G=
XP_005264234.1:n.*8G=
XM_011532662.2:c.*8G=
XP_011530964.1:n.*8G=
XM_011532663.2:c.*8G=
XP_011530965.1:n.*8G=
XM_011532666.2:c.*8G=
XP_011530968.1:n.*8G=
XM_011532667.3:c.*8G=
XP_011530969.1:n.*8G=
XM_017003526.1:c.*8G=
XP_016859015.1:n.*8G=
XM_017003527.1:c.*8G=
XP_016859016.1:n.*8G=
XR_001738657.1:n.2954G=
NM_001375819.1:c.*8G=
NP_001362748.1:n.*8G=
NR_135490.2:n.3177G=
NM_022552.5:c.*8G=
MANE Select
NP_072046.2:n.*8G=