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Genomic Alleles
HGVS
Genome Assembly
NC_000001.11:g.151612282G= , CM000663.2:g.151612282G=
GRCh38
NC_000001.10:g.151584758G= , CM000663.1:g.151584758G=
GRCh37
NC_000001.9:g.149851382G=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000368841.7:c.81G=
ENSP00000357834.2:p.Gly27=
ENST00000368843.8:c.81G=
ENSP00000357836.3:p.Gly27=
ENST00000458013.7:c.81G=
MANE Select
ENSP00000400333.2:p.Gly27=
ENST00000642376.1:c.81G=
ENSP00000496645.1:p.Gly27=
ENST00000642479.1:c.81G=
ENSP00000496775.1:p.Gly27=
ENST00000368841.6:c.81G=
ENSP00000357834.2:p.Gly27=
ENST00000368843.7:c.81G=
ENSP00000357836.3:p.Gly27=
ENST00000458013.6:c.81G=
ENSP00000400333.2:p.Gly27=
NM_030918.5:c.81G=
NP_112180.4:p.Gly27=
XM_005245509.1:c.81G=
XP_005245566.1:p.Gly27=
XM_005245511.3:c.-347G=
XP_005245568.1:n.-347G=
XM_011510024.1:c.81G=
XP_011508326.1:p.Gly27=
XM_011510025.1:c.81G=
XP_011508327.1:p.Gly27=
XM_011510026.1:c.81G=
XP_011508328.1:p.Gly27=
NM_001330723.1:c.81G=
NP_001317652.1:p.Gly27=
XM_005245511.4:c.-347G=
XP_005245568.1:n.-347G=
XM_011510024.2:c.81G=
XP_011508326.1:p.Gly27=
XM_011510025.2:c.81G=
XP_011508327.1:p.Gly27=
XM_011510026.2:c.81G=
XP_011508328.1:p.Gly27=
XM_017002417.1:c.81G=
XP_016857906.1:p.Gly27=
XM_024450038.1:c.-246G=
XP_024305806.1:n.-246G=
NM_001330723.2:c.81G=
MANE Select
NP_001317652.1:p.Gly27=
NM_030918.6:c.81G=
NP_112180.4:p.Gly27=