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Genomic Alleles
HGVS
Genome Assembly
NC_000011.10:g.116830637C= , CM000673.2:g.116830637C=
GRCh38
NC_000011.9:g.116701353C= , CM000673.1:g.116701353C=
GRCh37
NC_000011.8:g.116206563C=
NCBI36
NG_008949.1:g.5730C=
Transcript Alleles
HGVS
Amino-acid Change
NM_000040.3:c.55C=
MANE Select
NP_000031.1:p.Arg19=
ENST00000227667.8:c.55C=
MANE Select
ENSP00000227667.2:p.Arg19=
NM_000040.1:c.55C=
NP_000031.1:p.Arg19=
NM_000040.2:c.55C=
NP_000031.1:p.Arg19=
ENST00000227667.7:c.55C=
ENSP00000227667.2:p.Arg19=
ENST00000375345.3:c.109C=
ENSP00000364494.1:p.Arg37=
ENST00000433777.5:c.55C=
ENSP00000410614.1:p.Arg19=
ENST00000470144.1:n.87C=
ENST00000630701.1:c.109C=
ENSP00000486182.1:p.Arg37=