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Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.616940C= , CM000673.2:g.616940C=
GRCh38
NC_000011.9:g.616940C= , CM000673.1:g.616940C=
GRCh37
NC_000011.8:g.606940C=
NCBI36
NG_029106.1:g.4060G=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000358353.8:c.*411G=
ENSP00000351118.4:n.*411G=
ENST00000397542.7:c.*411G=
MANE Select
ENSP00000380676.2:n.*411G=
ENST00000358353.7:c.*411G=
ENSP00000351118.3:n.*411G=
ENST00000397542.6:c.*411G=
ENSP00000380676.2:n.*411G=
NM_001171968.1:c.*411G=
NP_001165439.1:n.*411G=
NM_021924.4:c.*411G=
NP_068743.2:n.*411G=
NM_031264.3:c.*411G=
NP_112554.2:n.*411G=
XM_006718253.2:c.*411G=
XP_006718316.1:n.*411G=
XM_011520188.1:c.*411G=
XP_011518490.1:n.*411G=
XM_011520189.1:c.*411G=
XP_011518491.1:n.*411G=
XM_011520190.1:c.*626G=
XP_011518492.1:n.*626G=
XM_006718253.3:c.*411G=
XP_006718316.1:n.*411G=
XM_011520188.2:c.*411G=
XP_011518490.1:n.*411G=
XM_011520189.2:c.*411G=
XP_011518491.1:n.*411G=
XM_011520190.2:c.*626G=
XP_011518492.1:n.*626G=
NM_001171968.2:c.*411G=
NP_001165439.2:n.*411G=
NM_021924.5:c.*411G=
MANE Select
NP_068743.3:n.*411G=
NM_031264.4:c.*411G=
NP_112554.3:n.*411G=
NM_001171968.3:c.*411G=
NP_001165439.2:n.*411G=
NM_031264.5:c.*411G=
NP_112554.3:n.*411G=