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Genomic Alleles
HGVS
Genome Assembly
NC_000016.10:g.3727686C= , CM000678.2:g.3727686C=
GRCh38
NC_000016.9:g.3777687C= , CM000678.1:g.3777687C=
GRCh37
NC_000016.8:g.3717688C=
NCBI36
NG_009873.1:g.157435G=
NG_009873.2:g.158028G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000262367.10:c.*32G=
MANE Select
ENSP00000262367.5:n.*32G=
ENST00000262367.9:c.*32G=
ENSP00000262367.5:n.*32G=
ENST00000382070.7:c.*32G=
ENSP00000371502.3:n.*32G=
NM_001079846.1:c.*32G=
NP_001073315.1:n.*32G=
NM_004380.2:c.*32G=
NP_004371.2:n.*32G=
XM_005255124.3:c.*32G=
XP_005255181.1:n.*32G=
XM_005255125.3:c.*32G=
XP_005255182.1:n.*32G=
XM_006720848.2:c.*32G=
XP_006720911.1:n.*32G=
XM_011522380.1:c.*32G=
XP_011520682.1:n.*32G=
XM_011522381.1:c.*32G=
XP_011520683.1:n.*32G=
XM_005255124.4:c.*32G=
XP_005255181.1:n.*32G=
XM_005255125.4:c.*32G=
XP_005255182.1:n.*32G=
XM_006720848.3:c.*32G=
XP_006720911.1:n.*32G=
XM_011522381.2:c.*32G=
XP_011520683.1:n.*32G=
XM_017022944.1:c.*32G=
XP_016878433.1:n.*32G=
NM_004380.3:c.*32G=
MANE Select
NP_004371.2:n.*32G=