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Genomic Alleles
HGVS
Genome Assembly
NC_000022.11:g.37185447C= , CM000684.2:g.37185447C=
GRCh38
NC_000022.10:g.37581487C= , CM000684.1:g.37581487C=
GRCh37
NC_000022.9:g.35911433C=
NCBI36
Transcript Alleles
HGVS
Amino-acid Change
ENST00000337843.7:c.60G=
MANE Select
ENSP00000338812.2:p.Met20=
ENST00000337843.6:c.60G=
ENSP00000338812.2:p.Met20=
ENST00000397110.6:c.60G=
ENSP00000380299.2:p.Met20=
ENST00000434784.1:c.60G=
ENSP00000399243.1:p.Met20=
ENST00000470655.5:n.3550G=
ENST00000493023.1:n.502G=
NM_031910.3:c.60G=
NP_114116.3:p.Met20=
NM_182486.1:c.60G=
NP_872292.1:p.Met20=
XM_006724125.2:c.3G=
XP_006724188.1:p.Met1=
XM_011529857.1:c.3G=
XP_011528159.1:p.Met1=
NM_001365878.1:c.3G=
NP_001352807.1:p.Met1=
XM_011529857.2:c.3G=
XP_011528159.1:p.Met1=
XM_017028569.1:c.60G=
XP_016884058.1:p.Met20=
XM_024452150.1:c.60G=
XP_024307918.1:p.Met20=
XM_024452151.1:c.60G=
XP_024307919.1:p.Met20=
XM_024452152.1:c.60G=
XP_024307920.1:p.Met20=
XM_024452153.1:c.60G=
XP_024307921.1:p.Met20=
XM_024452154.1:c.60G=
XP_024307922.1:p.Met20=
XM_024452155.1:c.3G=
XP_024307923.1:p.Met1=
NM_031910.4:c.60G=
MANE Select
NP_114116.3:p.Met20=
NM_182486.2:c.60G=
NP_872292.1:p.Met20=