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Genomic Alleles
HGVS
Genome Assembly
NC_000003.12:g.114171984A>G , CM000665.2:g.114171984A>G
GRCh38
NC_000003.11:g.113890831A>G , CM000665.1:g.113890831A>G
GRCh37
NC_000003.10:g.115373521A>G
NCBI36
NG_008842.2:g.32424T>C
Transcript Alleles
HGVS
Amino-acid Change
ENST00000698213.1:c.9T>C
ENSP00000513607.1:p.Ser3=
ENST00000383673.5:c.9T>C
MANE Select
ENSP00000373169.2:p.Ser3=
ENST00000295881.9:c.9T>C
ENSP00000295881.6:p.Ser3=
ENST00000383673.4:c.9T>C
ENSP00000373169.2:p.Ser3=
ENST00000460779.5:c.9T>C
ENSP00000419402.1:p.Ser3=
ENST00000467632.5:c.9T>C
ENSP00000420662.1:p.Ser3=
NM_000796.5:c.9T>C
NP_000787.2:p.Ser3=
NM_001282563.2:c.9T>C
NP_001269492.1:p.Ser3=
NM_001290809.1:c.9T>C
NP_001277738.1:p.Ser3=
NM_033663.5:c.9T>C
NP_387512.3:p.Ser3=
XM_011512510.1:c.9T>C
XP_011510812.1:p.Ser3=
XM_011512511.1:c.9T>C
XP_011510813.1:p.Ser3=
XM_011512512.1:c.9T>C
XP_011510814.1:p.Ser3=
XM_017005829.1:c.9T>C
XP_016861318.1:p.Ser3=
NM_000796.6:c.9T>C
MANE Select
NP_000787.2:p.Ser3=
NM_033663.6:c.9T>C
NP_387512.3:p.Ser3=