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Genomic Alleles
HGVS
Genome Assembly
NC_000002.12:g.238397580T= , CM000664.2:g.238397580T=
GRCh38
NC_000002.11:g.239306221T= , CM000664.1:g.239306221T=
GRCh37
NC_000002.10:g.238970960T=
NCBI36
NG_053055.1:g.82092T=
Transcript Alleles
HGVS
Amino-acid Change
ENST00000373327.5:c.1811T=
MANE Select
ENSP00000362424.4:p.Met604=
ENST00000373327.4:c.1811T=
ENSP00000362424.4:p.Met604=
ENST00000391993.7:c.1613T=
ENSP00000375851.3:p.Met538=
ENST00000462122.1:n.822T=
ENST00000483951.1:n.159T=
NM_001139490.1:c.1613T=
NP_001132962.1:p.Met538=
NM_015650.3:c.1811T=
NP_056465.2:p.Met604=
XM_006712414.1:c.1610T=
XP_006712477.1:p.Met537=
XM_011510944.1:c.1913T=
XP_011509246.1:p.Met638=
XM_011510945.1:c.1874T=
XP_011509247.1:p.Met625=
XM_011510946.1:c.1841T=
XP_011509248.1:p.Met614=
XM_011510947.1:c.1781T=
XP_011509249.1:p.Met594=
XM_011510948.1:c.1715T=
XP_011509250.1:p.Met572=
XM_011510950.1:c.779T=
XP_011509252.1:p.Met260=
XM_006712414.2:c.1610T=
XP_006712477.1:p.Met537=
XM_011510944.2:c.1913T=
XP_011509246.1:p.Met638=
XM_011510945.2:c.1874T=
XP_011509247.1:p.Met625=
XM_011510946.2:c.1841T=
XP_011509248.1:p.Met614=
XM_011510947.2:c.1781T=
XP_011509249.1:p.Met594=
XM_011510948.2:c.1715T=
XP_011509250.1:p.Met572=
XM_011510950.2:c.779T=
XP_011509252.1:p.Met260=
XM_017003789.1:c.1910T=
XP_016859278.1:p.Met637=
XR_001738696.1:n.1639T=
XR_001738697.1:n.1636T=
NM_015650.4:c.1811T=
MANE Select
NP_056465.2:p.Met604=