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Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.68348188C= , CM000673.2:g.68348188C=
GRCh38
NC_000011.9:g.68115656C= , CM000673.1:g.68115656C=
GRCh37
NC_000011.8:g.67872232C=
NCBI36
NG_015835.1:g.40549C=
NG_015835.2:g.40549C=
Transcript Alleles
HGVS
Amino-acid Change
NM_002335.4:c.433C=
MANE Select
NP_002326.2:p.Leu145=
ENST00000294304.12:c.433C=
MANE Select
ENSP00000294304.6:p.Leu145=
NM_001291902.1:c.-1333C=
NP_001278831.1:n.-1333C=
NM_001291902.2:c.-1333C=
NP_001278831.1:n.-1333C=
NM_002335.3:c.433C=
NP_002326.2:p.Leu145=
ENST00000294304.11:c.433C=
ENSP00000294304.6:p.Leu145=
ENST00000529993.5:c.433C=
ENSP00000436652.1:p.Leu145=
XM_005273994.2:c.433C=
XP_005274051.1:p.Leu145=
XM_011545029.1:c.460C=
XP_011543331.1:p.Leu154=
XM_011545030.1:c.460C=
XP_011543332.1:p.Leu154=
XM_011545031.1:c.460C=
XP_011543333.1:p.Leu154=
XR_001747874.1:n.475C=
XR_949925.1:n.475C=
XR_949925.2:n.475C=
XR_949926.1:n.475C=
XR_949926.2:n.475C=