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Genomic Alleles
HGVS
Genome Assembly
NC_000012.12:g.116237702C= , CM000674.2:g.116237702C=
GRCh38
NC_000012.11:g.116675507C= , CM000674.1:g.116675507C=
GRCh37
NC_000012.10:g.115159890C=
NCBI36
NG_023366.1:g.44485G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000281928.9:c.76G=
MANE Select
ENSP00000281928.3:p.Glu26=
ENST00000548743.2:c.46G=
ENSP00000448553.2:p.Glu16=
ENST00000551197.2:c.26G=
ENST00000650226.1:c.76G=
ENSP00000496981.1:p.Glu26=
ENST00000650375.1:n.238G=
ENST00000281928.7:c.76G=
ENSP00000281928.3:p.Glu26=
ENST00000548743.1:c.46G=
ENSP00000448553.1:p.Glu16=
ENST00000551197.1:n.26G=
NM_015335.4:c.76G=
NP_056150.1:p.Glu26=
XM_011538080.1:c.76G=
XP_011536382.1:p.Glu26=
XM_011538081.1:c.76G=
XP_011536383.1:p.Glu26=
XM_011538082.1:c.46G=
XP_011536384.1:p.Glu16=
XM_011538080.2:c.76G=
XP_011536382.1:p.Glu26=
XM_011538081.2:c.76G=
XP_011536383.1:p.Glu26=
XM_011538082.2:c.46G=
XP_011536384.1:p.Glu16=
XM_017019090.1:c.76G=
XP_016874579.1:p.Glu26=
NM_015335.5:c.76G=
MANE Select
NP_056150.1:p.Glu26=