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Genomic Alleles
HGVS
Genome Assembly
NC_000006.12:g.31616137G= , CM000668.2:g.31616137G=
GRCh38
NC_000006.11:g.31583914G= , CM000668.1:g.31583914G=
GRCh37
NC_000006.10:g.31691893G=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000376059.8:c.188G=
MANE Select
ENSP00000365227.3:p.Gly63=
ENST00000337917.11:c.230G=
ENSP00000338776.7:p.Gly77=
ENST00000376049.4:c.26G=
ENSP00000365217.4:p.Gly9=
ENST00000376059.7:c.188G=
ENSP00000365227.3:p.Gly63=
ENST00000466820.1:n.605G=
ENST00000497362.5:n.607G=
NM_001623.3:c.188G=
NP_001614.3:p.Gly63=
NM_004847.3:c.26G=
NP_004838.1:p.Gly9=
NM_032955.1:c.26G=
NP_116573.1:p.Gly9=
XM_005248870.3:c.188G=
XP_005248927.1:p.Gly63=
XM_005248871.1:c.251G=
XP_005248928.1:p.Gly84=
NM_001318970.1:c.26G=
NP_001305899.1:p.Gly9=
NM_001623.4:c.188G=
NP_001614.3:p.Gly63=
NM_032955.2:c.26G=
NP_116573.1:p.Gly9=
XM_005248870.4:c.188G=
XP_005248927.1:p.Gly63=
XM_017010332.1:c.26G=
XP_016865821.1:p.Gly9=
NM_001623.5:c.188G=
MANE Select
NP_001614.3:p.Gly63=
NM_001318970.2:c.26G=
NP_001305899.1:p.Gly9=
NM_032955.3:c.26G=
NP_116573.1:p.Gly9=