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Genomic Alleles
HGVS
Genome Assembly
NC_000005.10:g.36953741G= , CM000667.2:g.36953741G=
GRCh38
NC_000005.9:g.36953843G= , CM000667.1:g.36953843G=
GRCh37
NC_000005.8:g.36989600G=
NCBI36
NG_006987.1:g.81859G=
NG_006987.2:g.81859G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000282516.13:c.45G=
MANE Select
ENSP00000282516.8:p.Gly15=
ENST00000652901.1:c.45G=
ENSP00000499536.1:p.Gly15=
ENST00000282516.12:c.45G=
ENSP00000282516.8:p.Gly15=
ENST00000448238.2:c.45G=
ENSP00000406266.2:p.Gly15=
ENST00000621733.1:c.-1+76719G=
ENSP00000480694.1:n.-1+76719G=
NM_015384.4:c.45G=
NP_056199.2:p.Gly15=
NM_133433.3:c.45G=
NP_597677.2:p.Gly15=
XM_005248280.2:c.45G=
XP_005248337.1:p.Gly15=
XM_006714467.2:c.45G=
XP_006714530.1:p.Gly15=
XM_006714468.1:c.45G=
XP_006714531.1:p.Gly15=
XM_011514014.1:c.45G=
XP_011512316.1:p.Gly15=
XM_011514015.1:c.45G=
XP_011512317.1:p.Gly15=
XM_005248280.3:c.45G=
XP_005248337.1:p.Gly15=
XM_006714468.2:c.45G=
XP_006714531.1:p.Gly15=
XM_017009329.1:c.45G=
XP_016864818.1:p.Gly15=
XM_017009331.1:c.45G=
XP_016864820.1:p.Gly15=
NM_133433.4:c.45G=
MANE Select
NP_597677.2:p.Gly15=
NM_015384.5:c.45G=
NP_056199.2:p.Gly15=