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Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.2171721G= , CM000673.2:g.2171721G=
GRCh38
NC_000011.9:g.2192951G= , CM000673.1:g.2192951G=
GRCh37
NC_000011.8:g.2149527G=
NCBI36
NG_008128.1:g.5085C=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000352909.8:c.66C=
MANE Select
ENSP00000325951.4:p.Asp22=
ENST00000324155.8:c.66C=
ENSP00000325831.3:p.Asp22=
ENST00000333684.9:c.66C=
ENSP00000328814.6:p.Asp22=
ENST00000352909.7:c.66C=
ENSP00000325951.3:p.Asp22=
ENST00000381168.7:c.66C=
ENSP00000370560.3:p.Asp22=
ENST00000381175.5:c.66C=
ENSP00000370567.1:p.Asp22=
ENST00000381178.5:c.66C=
ENSP00000370571.1:p.Asp22=
NM_000360.3:c.66C=
NP_000351.2:p.Asp22=
NM_199292.2:c.66C=
NP_954986.2:p.Asp22=
NM_199293.2:c.66C=
NP_954987.2:p.Asp22=
XM_011520335.1:c.66C=
XP_011518637.1:p.Asp22=
XM_011520335.2:c.66C=
XP_011518637.1:p.Asp22=
NM_000360.4:c.66C=
MANE Select
NP_000351.2:p.Asp22=
NM_199292.3:c.66C=
NP_954986.2:p.Asp22=
NM_199293.3:c.66C=
NP_954987.2:p.Asp22=